Emerging Application of Pluot in Nutraceutical and Cosmetic Formulation
Roshani D. Bagul1, Sushant M. Ahire2, Deepak D. Sonwane3, Sunil K. Mahajan4
1,3Department of Pharmaceutics, Divine College of Pharmacy Satana, Nashik, Maharashtra, India.
2,4Department of Pharmaceutical Chemistry, Divine College of Pharmacy Satana, Nashik, Maharashtra, India.
*Corresponding Author E-mail: sushantahire071@gmail.com
ABSTRACT:
Plumcots, pluots, and apriums are the products of successful backcrosses between plums and apricots. The agro-morphology, genotyping, bioactive compounds, and nutritional value of the genus Prunus, and specifically plums and apricots, are well-documented, according to a subject search on plums, apricots, and plumcots. However, only a small number of studies partially addressed the subject of the metabolomics of plum-apricot hybrids when search results for the years 2010–2023 were examined. Less than ten publications each year about plum-apricot hybrids were found in Scopus, 618 papers were located on Google Scholar (2010–2023), and only two results were found in PubMed for the same time using the same keywords, according to a database search. this demonstrates the enormous research potential and the necessity of offering a comprehensive chemical characterisation of the current hybrids of plum and apricot. The purpose of this review is to schematise the information that is currently available about plum-apricot hybrids (in relation to their parents), identify any gaps regarding their bioactive compounds, antioxidant activities, and health-promoting qualities, and suggest future directions for fruit hybrid characterisation. Antioxidants, vitamins A, C, and E, and natural fruit acids found in pluots help nourish, hydrate, and revitalise skin. The mask's goal is to offer a chemical-free skincare substitute that encourages healthier, smoother, and more radiant skin. The pluot face mask exhibits efficient moisturising and exfoliating qualities that are appropriate for different skin types thanks to the extraction and blending of natural substances. The results demonstrate the potential of pluot-based skincare products as advantageous and sustainable supplements to contemporary cosmetic procedures.
KEYWORDS: Fruit, Climacteric, Prunus, Polyphenols, Plant-Based, and Sugar.
INTRODUCTION:
A number of species, including apricots, plums, peaches, and cherries, are included in the genus Prunus, which includes fruits that are highly favoured for ingestion1. The goal of breeding programs is frequently to produce fruit with improved physical characteristics, such as a higher yield and, typically, a higher sugar content2. Genetic variability is a prerequisite for novel varieties, and the species Prunus provides such circumstances3. The two plum species that are currently most widely grown are the European and Japanese varieties.4 There are only a few types of the apricot tree, which is far less common5. In terms of economic significance, apricots come in third place, behind peaches and plums6.
The search for new varieties and interspecific hybrids is prompted by the high commercial value of Prunus fruits. The plum population contains a wide range of genotypes, according to research7. Plums and apricots are successful backcrosses. Around 2012, the first hybrid of plum and apricot was created8. A hybrid between an apricot and a plum may produce a An aprium, which is 25% plum and 75% apricot genetically and morphologically;9 a pluot, which has more plum than apricot traits; and a plumcot, which is an interspecific hybrid of Japanese plum and apricot.10
The pollination processes of plumcots and pluots are different; the former is self-fertile, while the latter need a pollinator. A distant analysis of the microsatellite markers of plums and pluots revealed that 51% of the 76 alleles in plumcots came from plums, but 83% of the alleles in pluots corresponded to plums.11 The interspecific plum × apricot hybrids can be grouped into five categories, according to a recent study.2 The same study also found that their morphology and agronomic behaviour were more similar to those of the plum than the apricot. Additionally, Szymajda et al. (2012)12 noted that the plum-apricot hybrids were more reliant on the plum genotype. The self-incompatibility alleles in commercially important plum and pluot cultivars with unknown incompatibility were found by Halasz et al. (2013).13
Some physical properties of plum-apricot hybrids, including tree and crown diameters, leaf characteristics, flowers, and bark, were thoroughly documented in research by Soldatov and Salas.14 A biometric assessment of the hybrid fruits was also provided by the same authors, who explained variations in the fruit's look and bearing potential. The physical characteristics of plum-apricot hybrids, including weight, size, fruit/pit ratio, and skin and flesh colour, were described by Yaman and Uzun.15
Searches of scientific databases yield the essential facts regarding the importance and accessibility of resources on a range of subjects. The scientific community has long studied fruits and thoroughly characterised them. Their phenological characteristics, genetic determinism, and metabolic and volatile profiles have all been extensively studied.17,18 Additionally, efforts have been undertaken to use fruit by-products in a variety of businesses in light of sustainable resource exploitation.19
As of right now, a topic search on plums, apricots, and plumcots revealed a wealth of literature regarding the agro-morphology, genotyping, bioactive compounds, and nutritional value of the genus Prunus, and specifically plums and apricots. However, only a small number of publications offered scientifically supported material on the subject of plum-apricot hybrids' metabolomics and biological activities when search results for the years 2010–2023 were examined. Less than ten publications each year on plum apricot hybrids were found in Scopus, according to searches in databases including PubMed, Google Scholar, and Scopus.
The phenology, morphology, and breeding plans of plum apricot hybrids were the main topics of 618 papers published on Google Scholar (2010–2023), while just two hits were obtained in PubMed for the same time period using the same keywords. This indicates a significant research gap and the requirement for in-depth investigations to offer a comprehensive chemical analysis of the current hybrids of plum and apricot.
The goal of this review is to systematise the knowledge that is currently available about plum-apricot hybrids, identify any gaps regarding their bioactive substances, antioxidant activities, and health-promoting qualities, and suggest future directions for fruit hybrid characterisation.
The segregation between Plum and Pluot according to organoleptic characters:
In the USA and various European nations, the per capita consumption of plums has either been constant or even declined over the past ten years. Plum consumption in the USA decreased from 0.64kg per capita annually in 2001 to 0.50kg per capita annually in 2004, which is less than that of European nations. Geographical location affects plum consumption in Italy, which ranges from 1.2 to 0.90kg per capita annually. For instance, consumers in the central region use 1.2kg, those in the northwest consume 1.14kg, and those in the south and islands consume 0.90kg. Customers complained about "off flavour," "lack of ripening," "astringent," "flesh browning," and textural traits linked to poor quality and frost damage on both continents.
Prices are not rising at the same time that production costs are. In California and other parts of the world, postharvest handling techniques with a focus on temperature management recommendations to prevent plum chilling injury have been suggested as part of the solution. Ripening protocols at the shipping and receiving end have been developed, promoted, and established in an effort to improve flavour or even add value to plums.
A number of postharvest physiologists and commercial businesses are working to develop and establish a general minimum quality index based on ripe soluble solids concentration (RSSC) and/or ripe titratable acidity (RTA) as a strategy to safeguard consumers and boost consumption. It has been asserted, although, that for certain plums, titratable acidity, distinctive flavour, scent, astringency, and texture are just as significant in determining customer approval as RSSC.
For a high acid, early dark plum, the interaction between RSSC and RTA has been clearly demonstrated. Specifically, within the same RSSC range (10.0-11.9%) combined with three RTA ranges (RTA ≤ 0.60%, RTA 0.61–0.99%, and RTA ≥ 1.00%), the mean degree of consumer liking decreased significantly (p<0.0001) as the RTA range increased to 6.2, 5.3, and 3.3, respectively. There have also been reports of this connection with early grapes.20
Fig.1: Segregation of Plum and Pluot20
Identification and Characterization of Plum and pluot Cultivars by Microsatellite Markers:
Pluots are hypothetical crosses between apricots (Prunus armeniaca L.) and plums (Prunus salicina Lindl.). In breeding and horticulture, the capacity to differentiate between plum and pluot cultivars is crucial. Using 28 microsatellite markers, we examined the genetic diversity of 14 plums, 6 pluots, and 1 plumcot that represent market cultivars in California. Seven apricot varieties were also examined. in order to find evidence of apricot in the ancestry of plumcot and pluots.
There was no parental material available for the original cross that gave rise to the pluot and plumcot. Three of the 28 SSR markers came from peaches (Prunus persica L.) and 25 from sweet cherries (Prunus avium L.). Transportability between these Prunus species was demonstrated by the fact that about 80% of the cherry primers produced amplification products in plum and pluots. The tested SSRs in plums and pluots showed one to eight putative alleles per locus. A total of 100 alleles were found in the plum and pluot samples, with an average of 4.3 alleles per primer combination. All examined cultivars were correctly distinguished using the SSR markers.
There were 76 alleles in pluots, of which 63(83%) were unique to plum, 9(12%) were shared by plum, pluots, and apricot, and no allele from apricot was detected in the pluots. 49 alleles were found in plumcot, of which 25 (51%) were specific to plum, 18(36%) to apricot, and 6 (12%) to plum, plumcot, and apricot. A dendrogram based on 168 SSR markers showed the relationships between the 28 cultivars of plum, pluot, and apricot. with pluot cultivars scattered among plum cultivars and more closely related to plum than to apricot, the dendrogram revealed that plums and pluots form a cluster apart from the apricots. Between the cluster of plums and apricots, Plumcot formed a distinct branch. These findings imply that SSR markers are useful instruments for plum diversity investigations and cultivar identification.21
Pharmacognosy of Pluot:
A hybrid fruit, a pluot is a cross between an apricot (Prunus armeniaca) and a plum (Prunus domestica or Prunus salicina). Floyd Zaiger, a plant breeder, popularised the trademarked term "pluot" in the late 20th century.
It is a member of the Rosaceae family Since pluot is a relatively recent, artificial hybrid created for commercial use, it lacks a direct or conventional pharmacognostic profile in pharmacognosy, the study of medical substances originating from natural sources. However, since both of its parent plants plum and apricot have established pharmacological and phytochemical characteristics, we may examine it using those characteristics.
Pharmacognostic Profile of Pluot (Inferred from Plum and Apricot):
1. Botanical Source:
A cross between Prunus armeniaca (apricot) and Prunus salicina (Japanese plum)
Family: Rosaceae.
2. Macroscopic Characteristics:
Smooth, thin skin that resembles a plum
Firm, delicious meat that combines the texture of an apricot and a plum
A variety of colours, including red, purple, yellow, and green Stone fruit (one hard seed)
3. Microscopic Characteristics:
Microscopic analysis (based on similar drupaceous fruits):
Unicellular trichomes in the epidermis0
Calcium oxalate crystals in the mesocarp's.
parenchymatous tissue Sclerenchyma cells in the stone Vascular bundles in the mesocarp and endocarp.
4. Phytochemical Constituents (Based on Plum and Apricot data):
5. Phenolic substances, such as gallic acid, catechins, and chlorogenic acid:
Quercetin and kaempferol are examples of flavonoids.
Anthocyanins, particularly in dark-coloured pluots, Ascorbic acid, or vitamin C Carotenoids particularly beta-carotene in forms that resemble apricots Fibre particularly pectin Triterpenoids
Sugars (fructose, glucose, and sucrose)
Organic acids, such as citric and malic acid
6. Pharmacological/Medicinal Properties (Inferred from Parent Fruits):
Table 1. Pharmacological and Medical Properties:22
|
Property |
Evidence |
Source |
|
Antioxidant |
High phenolic and anthocyanin content |
Plum, apricot |
|
Anti-inflammatory |
Polyphenols and flavonoids |
Plum |
|
Anticancer potential |
Extracts from plums have shown effects on cancer cell lines in vitro |
Research studies |
|
Hypoglycemic |
Plum and apricot may help regulate blood sugar |
Animal models |
|
Digestive aid |
Rich in fiber and sorbitol promotes bowel movement |
Plum |
|
Hepatoprotective |
Apricot extracts shown to protect liver in studies |
Animal studies |
7. Uses in Traditional Medicine:
Because pluot is a modern hybrid, it has no traditional usage, however its parents are utilised in ethnomedicine:
Plum: Used for inflammation, fever, and constipation. Apricot: Used for digestion, skin care, and occasionally for respiratory problems in traditional Chinese medicine.
8. Toxicology:
Amygdalin, a cyanogenic glycoside that can produce cyanide when hydrolysed, may be present in seed kernels, such as those found in apricots and plums.
It is not advised to eat kernels.
9. Potential Applications:
Functional foods and nutraceuticals
Natural antioxidant sources
the cosmetic sector (because of vitamins and antioxidants).22
Metabolic Profile, Bioactive Compounds, and Antioxidant Capacity:
A variety of techniques have been used to characterise apricots and plums, including ripening, cultivar, and storage changes. Nevertheless, the chemical composition and bioactivity of plum-apricot hybrids have not yet been determined. The chemical makeup of apricot plum hybrids has only been partially described in a few numbers of publications. This prompts researchers to collect data on the parents of the hybrids, anticipating that they will possess some or all of the described characteristics with varying quantities. In light of the current dearth of publications in this specific topic, the strategy used in this work is to systematise the material now available regarding the chemical and bioactive substances identified in both plums and apricots in order to create grounds for future hybrid examination.
Among the main metabolites found in fruits are sugars, lipids, amino acids, and organic acids.23 Different fruits have been shown to have different levels of both sugar and organic acid.24 Studies found that oxalic and quinic acids were substantially connected in plumcots and plums, whereas oxalic and malic acids were greatly correlated with shikimic acid in apricots and plumcots.25
Plums have the highest concentrations of citric and malic acids.26 It has been reported that malic acid has improved chemical-bioactive qualities.27 Papers classify organic acids into three groups:28 tartaric acid, quinic acid (shikimic route), and anions of citric, isocitric, and malic acids (Krebs cycle intermediates). Soluble sugars are an essential part of the fruit pulp and are crucial to the flavour of fresh fruit.29 As fruit develops, its sugar content varies.30 The sugar content of fruit is most frequently reported to include glucose, fructose, and sucrose.31
Table 2. Partial chemical composition and bioactive compounds of plums, apricots, and hybrids.31
|
Constituent Type |
Plum (Prunus domestica) |
Apricot (Prunus armeniaca) |
Pluot (Plum × Apricot hybrid) |
|
Main Sugars |
Glucose, fructose, sucrose, sorbitol |
Sucrose, glucose, fructose |
Fructose, glucose, sucrose, sorbitol |
|
Organic Acids |
Malic acid, citric acid |
Citric, malic, tartaric acids |
Malic acid (dominant) citric acid |
|
Vitamin A (β-carotene) |
Moderate |
High |
Moderate |
|
Vitamin C |
Moderate to high |
Moderate |
Moderate to high |
|
Vitamin K |
Moderate |
Low to moderate |
Moderate |
|
Vitamin E |
Low to moderate |
Moderate |
Moderate |
|
B Vitamins |
B1, B2, B6, folate |
B1, B2, niacin |
Mix from both parents |
|
Potassium |
High |
High |
High |
|
Other Minerals |
Magnesium, calcium, iron |
Calcium, phosphorus, iron |
Magnesium, calcium |
|
Phenolic Compounds |
Chlorogenic acid, neochlorogenic acid, quercetin, kaempferol |
Chlorogenic acid, ferulic acid, catechin, quercetin |
Mixed profile of parents |
|
Anthocyanins |
High (in dark-skinned varieties) |
Low |
Moderate to high (variety-dependent) |
|
Carotenoids |
Low |
High (β-carotene, zeaxanthin) |
Moderate (orange flesh) |
|
Dietary Fiber |
High (especially in prunes) |
Moderate |
Moderate |
|
Aromatic Compounds |
Benzaldehyde, linalool, hexanal |
Linalool, benzaldehyde |
Mix of plum and apricot aroma compounds |
The literature on apricots reports a high fructose (40.79 mg/100g) and glucose (44.53mg/100g) content, noting that cultivar variations cause the sugar level to fluctuate.32 The entire amount of sugar plus a tiny amount of other organic compounds make up the majority of the total soluble solids parameter.33 Shamsolshoara et al.34 described three hybrids and discovered notable variations in their titratable acidity (2.6 to 4.6) and total soluble solids (16.8 to 20.2 Brix). Although most fruits have a modest lipid content, the fatty acid components may offer some health advantages.35 Oleic (43.9-78.5%), linoleic (9.7-37%), and palmitic (4.9-7.3%) acids were the primary fatty acids found in Prunus spp. kernel oils.36 Palmitoleic (0.08–0.32%), palmitic (27.27-32.70%), linolenic (11.47-17.16%), linoleic (42.09-46.99%), oleic (1.32-4.64%), and stearic (2.83-4.15%) were the most common fatty acids found in P. armeniaca L. kernel extracts.37 Apricot fruit's total lipid content ranged from 0.30 to 0.88g/100g FW.38 The fatty acids that were most prevalent were linoleic, palmitic, and linolenic, which is similar to the kernels. Linoleic, Cis-11-eicosanoic, and palmitic acids were the main fatty acids present in plums.39
There is no denying the importance of fruits in terms of vitamins and minerals. Fruits can acquire varying levels of metabolites depending on a number of parameters (temperature, rain, fertilisers, cultivars, sunlight hours, etc.).40 Vitamin C, carotenoids, and numerous B-group vitamins are typically abundant in fruits.41 One excellent source of calcium, phosphorus, and niacin is dried apricots33 the human body's metabolic processes depend on ascorbic acid, which has been found in both plums and apricots (Table 1).42
Plums were found to have a total ascorbic acid concentration of 454mg/100g FW.39 Three primary carotenoids were found in apricots: β-carotene (2% to 67% of the total carotenoid concentration), phytoene (6–59%), and phytofluene (12–45%).43
Vitamins, carotenoids, polyphenols (flavonoids and phenolic acids), and minerals are the four primary subgroups of the non-enzymatic natural antioxidants found in fruits.44 Plant matrices include a wide variety of phenolic chemicals.45
Support for foods high in natural antioxidants is needed since free radicals are increasingly thought to be the cause of oxidative stress, ageing, and a number of diseases.46 There are a lot of data in the literature about the antioxidant activity of Prunus spp.47
While the overall anthocyanin and flavonoid levels are higher in the fruit skin and much lower in the fruit pulp, the plum fruit contains a considerable amount of total phenolics.48 The "Stanley" plum's total phenolic content ranged from 70 to 214mg gallic acid equivalents/100g fresh weight44 Additionally, compared to apricot pulp, apricot peels contain more procyanidin, hydroxycinnamic acid, and flavonols.49 Polyphenols (165.49mg of GAE/100 g DM) and flavonoids (12.11 mg of QE/100g DM) are abundant in fresh apricot fruits.50 RP-UHPLC has been used to identify catechin, quercetin-rutinoside, and quercetin-rhamnoside in plums.51
A P. domestica × P. salicina hybrid was found to have a total antioxidant activity of 809.5mg TE/100g.52 Genotype differences in hybrid DPPH antioxidant activity were shown to range from 42.4 to 60%.34
The same authors proposed that, in relation to some substances like anthocyanins and phenolics, the colour of the flesh may be associated with antioxidant activity. Drogoudi and Pantelidis examined the antioxidant content and fruit morphological characteristics of 43 plum varieties, including one pluot.53
The total soluble solids (TSS) value of the investigated pluot was 18.6 Brix,
and its antioxidant activity, as determined by DPPH and FRAP techniques, was
similar to that of the "Santa Rosa" plum cultivar. The results of
Alajil et al. examining the antioxidant activity of apricots assessed using the
three methods further corroborate the claim that the CUPRAC approach is more
sensitive in the presence of flavonoids (quercetin and kaempferol).54
Some of the detected lipids, amino acids and their derivatives, organic acids, saccharides and alcohols, nucleotides, and vitamins increase with storage, changing the metabolic profiles of plums.55 Variations in the sugar level, total phenolic content, and antioxidant activity at various stages of plum ripening have also been documented by other authors.56 There was no discernible pattern for a rise or fall in the parameters. Changes in the metabolite content, however, should be considered, particularly in relation to the fruit harvesting season.
The identification of important fragrance components in different matrices is aided by volatile investigations. There is currently no material accessible on the subject of plum-apricot hybrid volatolomics, which offers an unexplored area for study. The volatile character of apricots and plums, however, has already been documented. 58 esters are the most prevalent of the 148 components found in fresh plums, according to Pino and Quijano's research.57
Ethyl 2-methylbutanoate, hexyl acetate, (E)-2-nonenal, ethyl butanoate, (E)-2-decenal, ethyl hexanoate, nonanal, decanal, linalool, γ-decalactone, butyl acetate, limonene, propyl acetate, δ-decalactone, diethyl sulphide, (E)-2-hexenyl acetate, ethyl heptanoate, (Z)-3-hexenol, (Z)-3-hexenyl hexanoate, eugenol, (E)-2-hexenal, ethyl pentanoate, and hexyl 2-methylbutanoate. Alcohols predominated among the far fewer chemicals (75 in total) reported for apricots.58 (E)-2-hexenol, (E)-2-hexenal, hexenal, benzyl alcohol, (Z)-3-hexenal, and y-caprolactone were the significant volatiles.
Amygdalin is a naturally occurring cyanogenic glycoside.59
that is present in a number of Prunus species.60 Its pharmacological and toxicological effects are the subject of increasing research.61 The genotype has a major impact on the amygdalin content, which varies greatly between bitter and sweet apricot kernels.62 Plum seeds also contain amygdalin.63 It's possible that the plum-apricot hybrids have varying concentrations of this cyanogenic glycoside, but no research has been done on the subject yet.
Given that plumcots and pluots share many characteristics with plums, it is possible that they will also share more chemical characteristics with plums. Future studies supporting this assumption would be interesting, particularly with regard to the concentration of polysaccharides, vitamins, minerals, and amino and phenolic acids. In the early stages of ripening, the organic acid content of apricots and plumcots is similar, and in the latter stages of ripening, it is similar to that of plums, according to a paper by Bae et al.25 Accordingly, apriums resemble apricots more, which could suggest that they are similar in composition. Once more, more research is required to confirm or deny the aforementioned hypotheses.
Health Beneficial Properties:
Phytochemicals are bioactive substances produced by secondary plant metabolism64 that are essential to oxidation and inflammatory processes.65 Carotenoids, glucosinolates, phytosterols, polyphenols, and saponins are only a few of the compounds that make up phytonutrients.66 By elucidating the method of action of their active constituents,67 phyto-nutrition uncovers how plant molecules can be included into a daily diet with positive health consequences.68 Because of their parents' enormous health benefits, plum-apricot hybrids pose a significant scientific challenge. More details about their biological activities and nutritional characteristics should be available.
anticipated positive qualities. The large audience does not now have access to any information regarding their advantageous qualities. The health benefits of plums and apricots as parents of plum-apricot hybrids are thus discussed in this section.
Prunus domestica has antioxidant, anticancer, antihyperglycemic, antihyperlipidemic, and anti-osteoporosis qualities, according to a thorough analysis of its medicinal and pharmacological potential.69 According to reports, apricots are beneficial for respiratory and digestive conditions, inflammation, and liver issues.70 Consuming apricots may have a beneficial effect on atherosclerosis, high cholesterol, high homocysteine, and hepatic steatosis.71
1. Antihyperlipidemic Properties (Cholesterol Control):
Numerous health advantages can result from eating a diet high in fruits and vegetables.72 Because of their metabolic characteristics, eating plums may be responsible for improving lipid profile parameters by reducing LDL and total cholesterol levels.73 Prunus species are thought to have both fibre and polyphenol components, which may help reduce cholesterol.74 By improving bile acid conversion and sterol release, dietary fibre can reduce cholesterol levels.43
2. Anticancer Properties:
Cancer cells come in a variety of forms. Numerous plant extracts are said to have the ability to slow the progression of cancer. The processes via which Prunus armeniaca L. has anticancer action. include a decrease in angiogenesis, a rise in antioxidant defence, and a decrease in tumour growth.75 Prunus armeniaca natural compounds have been shown to be effective against a variety of cancers, lessen liver damage, act as cardio- and neuroprotectants by boosting antioxidant defence through glutathione, catalase, and superoxide dismutase, and lower pro-inflammatory cytokine levels.76
A thorough analysis of Prunus domestic’s pharmacological and therapeutic potential demonstrated its anticancer qualities by slowing the proliferation of cancer cells.58 Leukaemia, human cervical carcinoma, colon carcinoma, and breast cancer cells, among other conditions, are treated with ethanol extracts, immature plum extracts, and antioxidant fractions of prunes, according to the same scientists. Protocatechuic acid has been proposed as a possible explanation for these characteristics.77 The liver, colorectal adenocarcinoma, and breast cell lines are the three cell lines against which the plum fruit has demonstrated anticancer action.78 There have also been reports of plum extracts, plum juices, and plum wines having anti-cancer properties.79
3. Anti-Osteoporosis Properties:
There is evidence that supplementing with dried plums (≤100g/daily) will improve bone mineral density.80 Twenty-four cell, animal, population, and clinical investigations are systematically reviewed in Wallace.81 All of this research demonstrates improvements in indices of bone health, including as alkaline phosphatase, bone alkaline phosphatase, and bone mineral density. Some of the published research also established minerals including calcium, phosphorus, and magnesium. Here, the established qualities may also be attributed to the polyphenolic profile of prunes.
4. Anti-Inflammatory Activities:
Fruits high in phenol typically have anti-inflammatory qualities due to a decrease in intracellular reactive oxygen species, which may suppress the inflammatory process by reducing nitric oxide synthesis.82 Because of its bioactive components (tocopherols, terpenoids, and phenolic compounds), apricot seeds are thought to have antioxidant, antibacterial, and anti-inflammatory properties.83
5. Gut Microbiota Support:
Although prunes are thought to preserve bowel function, little study has been done on how Prunus domestica supports the gut bacteria on the gastrointestinal system. Consuming dried plums increased stool weight and frequency in healthy people with low fibre intake, as demonstrated by Lever et al.84 Another study found that a 12-month dietary supplement of prunes (50–100g/day) changed the gut microbiome by reducing the evenness of bacterial taxa.85 Prune supplementation enhanced the growth of Bifidobacteria, according to an updated assessment of Alasalvar et al. on the impact of dried fruit on the microbiome.86
6. Enzyme Inhibition (Antihyperglycemic and Neuroprotective Activities:
Poor food choices are linked to a modern lifestyle, which can manifest as insulin resistance, type II diabetes, obesity, and overweight, among other conditions.87 The scientific community values plant extracts' capacity to block the activity of certain enzymes. Specifically, the ability of plant extracts to inhibit α-glucosidase, α-amylase, and lipase is one of the most popular assays used in research to potentially find anti-obesity and antidiabetic medications.88 The search for novel sources of bioactive compounds that can be effectively integrated into drug discovery processes is being prompted by the goal of prevention through diet. Many Prunus species. have been shown to be capable of inhibiting the activity of many enzymes, including lipase, acetylcholinesterase, α-amylase, α-glucosidase, and tyrosinase. Important glycolytic enzyme activity has been shown to be inhibited by polyphenol-enriched extracts.89 The bitter apricot kernel aqueous extract demonstrated potent in vitro acetylcholinesterase inhibitory and neuroprotective properties, according to a study by Vahedi-Mazdabadi et al.90
Applications:
Fruit production is used in a variety of businesses, including pharmacy, culinary technology, and cosmetics, in addition to the direct ingestion of the ripe fruit. As the demand for a sustainable life cycle grows, fruit and vegetable by-products are currently a popular research area.
Fig.2: Presents the applications of Prunus spp. in different fields95
Making jams, marmalades, syrups, nectars, and other fruit conservation techniques including compote and fruit drying are obvious uses for fruit. For example, the chemical makeup of plum jams is a good source of nutrition and health benefits. Plum wines with different qualities have also been the subject of authors.91,92 Dried plums are thought to be profitable for use in meat products because of their unique qualities, such as lipid oxidant inhibition.93 The use of plum peels in halva Masghati has also been studied.94 Fruit preservation techniques include convective drying and osmotic dehydration.95
Researchers have examined how drying circumstances affect fruit quality using convective airflow drying, freezing, freeze drying, and swell drying. They have found that while these methods seem to work, further research is required to improve them.96 Because of their high protein and mineral content, apricot kernels are used to make an apricot, peach, and mango flour mixture that is added to baked foods.97 Apricot seed waste is used to make food emulsifiers and stabilisers, which are intriguing natural compounds with potential industrial and medical uses.98
The stability of plum fruit phenolic extracts via microencapsulation has been studied by authors, who note that this is a promising method that needs more research on how plum phenolics interact with other food ingredients.99
Since most plant matrices contain polyphenols, a variety of fruit extracts are used as components in the field of cosmetology. Body wash compositions have effectively included prunus extracts as active ingredients. In an effort to increase the shelf life of edible coatings,100 plant extracts with unique antioxidant qualities have also been used.101 Because of its anti-aging qualities and overall brightening effect, kernel oils have long been utilised to treat conditions including dermatitis. Apricot seeds have been shown in studies to have dietary and cosmetic uses. There have been reports of apricots exhibiting antibacterial action, particularly against skin conditions.102,103
The topic of fruit by-product valorisation and its applications in several industries is currently receiving a lot of interest. Apricot waste can be a significant source of bioactive substances, according to a recent study that examined apricot pulp waste as a source of carotenoid pigments and antioxidant polyphenols.104 Another study emphasised that because of their antibacterial and antioxidant properties, plum by-products can be reintegrated into the food supply chain in light of the circular economy.105 It has been observed that a 2-propanol extract from apricot pomace inhibits the corrosion of mild steel.106
Because plum-apricot hybrids fully resemble their parents in both morphology and phenology, all of the aforementioned applications can be successfully applied to them. However, in order for any claim to be fully backed by scientific data, additional topic (plum-apricot hybrid) research and publication of the results are required.106
Pluot's Role in Cosmetic Formulations:
The following characteristics of pluots, which are rich in bioactive chemicals, make them potentially useful in cosmetics:
1. Antioxidant Properties:
Anthocyanins, flavonoids, and vitamin C found in plants aid in the neutralisation of free radicals. This can shield skin from environmental harm and early ageing.
2. Skin Brightening & Anti-aging:
Vitamin C enhances skin tone and promotes the production of collagen. Phenolic chemicals aid in the reduction of wrinkles and fine lines.
3. Moisturizing Effect: The fruit's organic acids and natural sugars can soften and moisturise the skin.
4. Anti-inflammatory & Soothing:
Reduces redness and puffiness and calms sensitive skin.
5. Fragrance and Color:
It can be used for mild tint and pleasant aroma in natural cosmetic lines.
6. Potential Applications:
· Face masks and washes
· Anti-aging creams
· Moisturisers
· Lip balms
· Natural skin-brightening products
· Brightening serums
· Sunscreen Booster
· Lip and eye care products.107
Face Mask:
The advantages of wearing masks are practically limitless, and they have been around for a very long time. These masks can be used to hydrate the skin, get rid of extra oil and pollutants, and make pores seem better. The sheet mask is made of materials like cellulose or microfibers. Because these face sheet masks are so affordable, anyone may use them with ease.108
· Deeply cleanse pores
· Eliminate more oil and debris
· Hydrate and moisturise the skin
· Brighten and improve skin tone
· Supply nutrients and active elements like vitamins or antioxidants.
Types of Face Masks include:
Clay masks – For oily or acne-prone skin.
Sheet masks – For moisture, use soaked in serum.
Gel masks – Calming and refreshing.
Cream masks– Hydrating for parched skin
Peel-off masks – get rid of blackheads and dead skin
Skin Benefits of Pluot in a Face Mask:
1. Rich in Antioxidants (like Vitamin C):
How it helps: It combats free radicals and lessens dullness and fine lines, which are indicators of ageing.
The mask's effect is to brighten skin and encourage a youthful shine.
2. Natural Alpha Hydroxy Acids (AHAs):
How it works: It loosens dead skin cells to gently exfoliate the skin.
Effect in mask: Smoother, softer skin with better texture
3. Vitamin A (from the apricot/plum lineage):
How it helps: promotes skin regeneration and cell turnover.
Effect in mask: skin that looks fresh and may be useful in treating acne.
4. Hydrating Sugars + Fiber:
How it helps: aids in keeping the skin hydrated.
Effect in mask: Skin feels more moisturised and plumper.
5. Mildly Astringent:
How it helps: It might help reduce oiliness and tighten pores.
Effect in mask: Skin appear more polished and less oily.109
Mechanism of Action of Pluot in Face Mask:
1. Antioxidant Protection:
Pluots are high in phenolic compounds, anthocyanins, and vitamin C, all of which aid in the battle against free radicals. By lowering oxidative stress, dullness, fine wrinkles, and early ageing are avoided.
2. Skin Brightening:
Pluots' natural fruit acids, which are similar to AHA, gently exfoliate dead skin cells.
Provides a natural shine and aids in improving skin tone.
3. Hydration & Moisturizing:
The high-water content of Pluot moisturises and revitalises the skin.
Reduces dryness and maintains the softness of the skin.
4. Anti-inflammatory Properties:
The bioactive substances lessen skin irritation, redness, and inflammation.
Ideal for skin that is sensitive or prone to acne.
5. Collagen Boosting:
Vitamin C increases the formation of collagen, which improves the firmness and suppleness of the skin.49
Method of Preparation of Face Mask:
Ingredients:
· One ripe pluot, peeled and mashed
· One teaspoon of natural moisturiser and antibacterial honey
· One spoonful of yoghurt or curd (for a calming and mild exfoliating effect)
Procedure:
1. Peel and wash the pluot fruit.
2. In a sanitised basin, mash the fruit pulp until it is smooth.
3. To the mashed fruit, add 1 teaspoon each of honey and yoghurt.
4. Create a smooth paste by thoroughly combining all the ingredients.
5. Evenly cover your clean face and neck with the mask.
6. Let it run for fifteen to twenty minutes.
7. Use lukewarm water to rinse, then pat dry.
Benefits:
Pluot: Packed with antioxidants and vitamins, it moisturises and enhances skin.
Honey: Provides moisture and combats bacteria.
Yoghurt: Gently exfoliates and calms skin.
For optimal effects, use two to three times each week.110
Future Perspectives:
One of the achievements of breeding initiatives is the creation of plum apricot hybrids. Even though the first plum-apricot hybrid emerged about ten years ago, nothing is known about the nutritional content, biological activity, and health-promoting qualities of these fruits. In contrast to the phenology, appearance, and breeding programs of plum-apricot hybrids, a topic search in scientific databases reveals little information regarding their chemical composition and related biological activity.
However, the parents of plumcot, pluot, and aprium (plums and apricots) are well-characterized, providing justification for anticipated health-promoting qualities and prominent compounds. This highlights a significant research gap and the necessity for in-depth investigations to fully characterise the chemical makeup and biological activity of the current plum-apricot hybrids. It is especially interesting to be able to apply the antioxidant, anticancer, antihyperglycemic, antihyperlipidemic, and anti-osteoporosis qualities that have been reported for plums and apricots to the hybrids. Foods with functional qualities are beneficial when seen through the lens of nutrition-based prevention.
Due to their lack of significant characterisation, hybrid fruits are rarely used in sustainable farming practices. More knowledge about sustainable agriculture systems in plant management may be required as a result of the European Green Deal's implementation. Immediate societal issues are created by worries about the high cost of maintenance and the requirement for rising food consumption. At the moment, hybrid orchards are only seen in research facilities. It is necessary to take steps to make them more popular and researched. Since many farmers are finding it difficult to fulfil market demands and are choosing to give up on their produce, sustainable farming methods must have a social component. When the market exerts immediate pressure, farmers may switch to more lucrative crops. Setting the record for current biodiversity is crucial because the world's biodiversity is continuously declining.107
Farmers and the scientific community might both greatly benefit from a database on fruit hybrids, which would make it easier to identify and characterise hybrid representatives. It might be challenging to compare and contrast findings in the literature because some hybrids may only be known by their common name.111
CONCLUSION:
There are currently databases for packed with vital nutrients, antioxidants, and bioactive substances, pluot fruit a special cross between plum and apricot offers several advantages for the skin. Its high vitamin C content improves skin suppleness and lessens indications of ageing by increasing the generation of collagen. Pluot's antioxidants fight free radicals, shielding the skin from oxidative damage and fostering a young appearance. Furthermore, dead skin cells are gently exfoliated by the natural acids, leaving the skin softer and more radiant. Pluot provides natural moisture, relieves inflammation, and promotes general skin health without the use of harsh chemicals in face masks. These characteristics make pluot-based face masks a cutting-edge, environmentally responsible, and successful choice in natural skincare formulas that are perfect for reviving and nourishing the skin. Pluot in face masks gives the skin natural hydration, nourishment, and antioxidant defence. Its abundance of vitamins, particularly A and C, helps to give skin a healthy glow, improve skin texture, and lessen indications of ageing. It is safe, mild, and efficient for routine skincare usage because it is a fruit-based product.
The pluot face mask exemplifies how natural fruit-based skincare can support glowing, healthy skin. The pluot, which is high in antioxidants, natural acids, and vitamins A, C, and E, helps nourish the skin, improve suppleness, and fight indications of ageing. It can be used on a variety of skin types because to its moisturising and exfoliating qualities, especially for reviving dry or dull skin. All things considered, the pluot face mask provides an efficient and ecological substitute for store-bought skincare products, demonstrating how natural components can promote wellness and beauty.
REFERENCE:
1. Mehlenbacher SA, Cociu V, Hough FL. Apricots (Prunus). In: Moore JN, Ballington JR Jr, editors. Genetic resources of temperate fruit and nut crops. Wageningen: ISHS; 1991. p. 65–110.
2. Sansavini S, Donati F, Costa F, Tartarini S. Advances in apple breeding for enhanced fruit quality and resistance to biotic stresses: new varieties for the European market. J Fruit Ornam Plant Res. 2004;12(Spec ed 2):13–52.
3. Brown WL. Genetic diversity and genetic vulnerability—an appraisal. Econ Bot. 1983;37(1):4–12.
4. Osorio M, Ahumada S, Infante R, Pacheco I, Fiol A, Ballesta P. A Japanese plum breeding core collection capturing and exploiting genetic variation. Agriculture. 2025;15(13):1369.
5. Easwaran V, Sadiq MM, Alavudeen SS, Alshahrani SM, Khan NA, Rajavardhana T, Pillai MS. Comparative analysis of knowledge, awareness and practice towards rational use of face masks between healthcare and non-healthcare individuals during the COVID-19 pandemic. Res J Pharm Technol. 2023;16(9):4281–7.
6. Zhebentyayeva T, Ledbetter C, Burgos L, Llácer G. Apricot. In: Badenes ML, Byrne DH, editors. Fruit breeding. Boston (MA): Springer; 2011. p. 415–58.
7. Gharaghani A, Solhjoo S. Varietal diversification of stone fruits. In: Gharaghani A, editor. Production technology of stone fruits. Singapore: Springer; 2021. p. 1–56.
8. Milošević T, Milošević N. Plum (Prunus spp.) breeding. In: Al-Khayri JM, Jain SM, Johnson DV, editors. Advances in plant breeding strategies: fruits. Vol. 3. Cham: Springer; 2018. p. 165–215.
9. Guerrero BI, Guerra ME, Herrera S, Irisarri P, Pina A, Rodrigo J. Genetic diversity and population structure of Japanese plum-type (hybrids of P. salicina) accessions assessed by SSR markers. Agronomy. 2021;11(9):1748.
10. Samir D, Manel A, Abir H. Phytochemical analysis and antioxidant property of rhizome aqueous extracts of Phragmites australis in alloxan diabetic rats. Liver. 2019; 4: 154.
11. Ahmad R, Potter D, Southwick SM. Identification and characterization of plum and pluot cultivars by microsatellite markers. J Hortic Sci Biotechnol. 2004; 79(1): 164–9.
12. Szymajda M, Studnicki M, Kuras A, Żurawicz E. Cross-compatibility in interspecific hybridization between three Prunus species. S Afr J Bot. 2022; 146: 624–33.
13. Halász J, Hegedűs A, Szabó Z, Nyéki J, Pedryc A. DNA-based S-genotyping of Japanese plum and pluot cultivars to clarify incompatibility relationships. HortScience. 2007; 42(1): 46–50.
14. Soldatov IV, Salaš P. Hybridization of domestic prunes with black apricot (Prunus domestica L. × Armeniaca dasycarpa Ehrh.). Acta Univ Agric Silvic Mendelianae Brun. 2007; 55(5): 147–54.
15. Suresh AS, Pawar B. A study of factors of lifestyle and its impact on nutraceutical consumption: India perspective. Asian J Manag. 2018;9(1):203–11.
16. Bai J, Jordán MJ, Li J. Metabolism of fruit volatile organic compounds. Front Plant Sci. 2022;13:873515.
17. Cosmulescu S, Ștefănescu D, Stoenescu AM. Variability of phenological behaviours of wild fruit tree species based on discriminant analysis. Plants. 2021;11(1):45.
18. Gallinat AS, Primack RB, Willis CG, Nordt B, Stevens AD, Fahey R, Whittemore AT, Du Y, Panchen ZA. Patterns and predictors of fleshy fruit phenology at five international botanical gardens. Am J Bot. 2018;105(11):1824–34.
19. Nirmal NP, Khanashyam AC, Mundanat AS, Shah K, Babu KS, Thorakkattu P, Al-Asmari F, Pandiselvam R. Valorization of fruit waste for bioactive compounds and their applications in the food industry. Foods. 2023;12(3):556.
20. Lokhande SS. Role of nutraceuticals in various diseases: A comprehensive review. Asian J Pharm Res. 2018;8(4):236–40.
21. Nicolás-Almansa M, Ruiz D, Guevara A, Cos J, Martínez-Gómez P, Rubio M. Genomic designing of new Plum pox virus resistant plumcot (Prunus salicina Lindl. × Prunus armeniaca L.) varieties through interspecific hybridization. In: Kole C, editor. Genomic designing for biotic stress resistant fruit crops. Cham: Springer; 2022. p. 287–304.
22. Kim DO, Chun OK, Kim YJ, Moon HY, Lee CY. Quantification of polyphenolics and their antioxidant capacity in fresh plums. J Agric Food Chem. 2003;51(22):6509–15.
23. Gu L, Zhang ZY, Quan H, Li MJ, Zhao FY, Xu YJ, Liu J, Sai M, Zheng WL, Lan XZ. Integrated analysis of transcriptomic and metabolomic data reveals critical metabolic pathways involved in rotenoid biosynthesis in the medicinal plant Mirabilis himalaica. Mol Genet Genomics. 2018;293(3):635–47.
24. Zhang J, Li J, Zhang H, Li Y, Farooq S, Bacha SA, Wang J. Evaluation of sugar and organic acid composition and their levels in highbush blueberries from two regions of China. J Integr Agric. 2020;19(9):2352–61.
25. Thakur S, Srivastava N. Nutraceuticals: A review. Asian J Res Pharm Sci. 2016;6(2):85–94.
26. Drkenda P, Mušić O, Oraš A, Haračić S, Haseljić S, Blanke M, Hudina M. Sugar, acid and phenols in fruit of the sharka-tolerant autochthonous plum genotype ‘Mrkosljiva’. Erwerbs-Obstbau. 2022;64(4):569–80.
27. Marques C, Sotiles AR, Farias FO, Oliveira G, Mitterer-Daltoe ML, Masson ML. Full physicochemical characterization of malic acid: Emphasis on its potential as a food ingredient and application in pectin gels. Arab J Chem. 2020;13(12):9118–29.
28. Famiani F, Battistelli A, Moscatello S, Cruz-Castillo JG, Walker RP. The organic acids that are accumulated in the flesh of fruits: occurrence, metabolism and factors affecting their contents—a review. Rev Chapingo Ser Hortic. 2015;21(2):97–128.
29. Cakpo CB, Vercambre G, Baldazzi V, Roch L, Dai Z, Valsesia P, Memah MM, Colombié S, Moing A, Gibon Y, Génard M. Model-assisted comparison of sugar accumulation patterns in ten fleshy fruits highlights differences between herbaceous and woody species. Ann Bot. 2020;126(3):455–70.
30. Anamika CV, Nautiyal A. A review: Health benefits of herbal plants in nutraceuticals. Asian J Pharm Technol. 2022; 12(3): 277–81.
31. Dai Z, Wu H, Baldazzi V, Van Leeuwen C, Bertin N, Gautier H, Wu B, Duchęne E, Gomčs E, Delrot S, Lescourret F. Inter-species comparative analysis of components of soluble sugar concentration in fleshy fruits. Front Plant Sci. 2016; 7: 649.
32. Zhivondov A, Uzundzhalieva K. Taxonomic classification of plum-apricot hybrids. In: XV International Symposium on Apricot Breeding and Culture. Acta Hortic. 2011;966:211–7.
33. Waseem M, Naqvi SA, Haider MS, Shahid M, Jaskani MJ, Khan IA, Abbas H. Antioxidant activity, sugar quantification, phytochemical and physical profiling of apricot varieties of Chitral and Gilgit-Pakistan. Pak J Bot. 2021;53(4):1–9.
34. Kusumiyati, Hadiwijaya Y, Putri IE, Mubarok S, Hamdani JS. Rapid and non-destructive prediction of total soluble solids of guava fruits at various storage periods using handheld near-infrared instrument. In: IOP Conf Ser Earth Environ Sci. 2020;458(1):012022.
35. Sarella PN, Mangam VT. Enhancing nutraceutical bioavailability with bilosomes: A comprehensive review. Asian J Pharm Technol. 2024;14(3):271–80.
36. Bajramova A, Spégel P. A comparative study of the fatty acid profile of common fruits and fruits claimed to confer health benefits. J Food Compos Anal. 2022;112:104657.
37. Matthaeus B, Oezcan MM. Fatty acids and tocopherol contents of some Prunus spp. kernel oils. J Food Lipids. 2009;16(2):187–99.
38. Hrichi S, Rigano F, Chaabane-Banaoues R, Oulad El Majdoub Y, Mangraviti D, Di Marco D, Babba H, Dugo P, Mondello L, Mighri Z, Cacciola F. Identification of fatty acid, lipid and polyphenol compounds from Prunus armeniaca L. kernel extracts. Foods. 2020;9(7):896.
39. Pintea A, Dulf FV, Bunea A, Socaci SA, Pop EA, Oprița VA, Giuffrida D, Cacciola F, Bartolomeo G, Mondello L. Carotenoids, fatty acids, and volatile compounds in apricot cultivars from Romania—a chemometric approach. Antioxidants. 2020;9(7):562.
40. Engla G, Khan MA. Studies on sun protection factor of sunscreen cosmetic formulations for their selection and use. Int J Pharm Sci Res. 2012;3:45–7.
41. Cheikhyoussef N. Profiling studies of five Namibian indigenous seed oils obtained using three different extraction methods [dissertation]. Windhoek: University of Namibia; Year unknown.
42. Murathan ZT, Arslan M, Erbil N. Analyzing biological properties of some plum genotypes grown in Turkey. Int J Fruit Sci. 2020;20(Suppl 3):S1729–40.
43. Pott DM, Vallarino JG, Osorio S. Metabolite changes during postharvest storage: Effects on fruit quality traits. Metabolites. 2020;10(5):187.
44. Rejman K, Górska-Warsewicz H, Kaczorowska J, Laskowski W. Nutritional significance of fruit and fruit products in the average Polish diet. Nutrients. 2021;13(6):2079.
45. Rajasekaran A, Sivagnanam G, Xavier R. Nutraceuticals as therapeutic agents: A review. Res J Pharm Technol. 2008;1(4):328–40.
46. Shemesh K, Zohar M, Hatib K, Holland D, Isaacson T. Analysis of carotenoids in fruit of different apricot accessions reveals large variability and highlights apricot as a rich source of phytoene and phytofluene. Fruits. 2017;72(4):185–202.
47. Walkowiak-Tomczak D, Reguła J, Łysiak G. Physico-chemical properties and antioxidant activity of selected plum cultivars fruit. Acta Sci Pol Technol Aliment. 2008;7(4):15–22.
48. Sadowska-Bartosz I, Bartosz G. Evaluation of the antioxidant capacity of food products: Methods, applications and limitations. Processes. 2022;10(10):2031.
49. Mihaylova D, Popova A, Dincheva I. Pattern recognition of varieties of peach fruit and pulp from their volatile components and metabolic profile using HS-SPME-GC/MS combined with multivariable statistical analysis. Plants. 2022;11(23):3219.
50. Mundhe AG, Dhapke P, Padole N, Dhoble N, Dod SR. Formulation and evaluation of nutraceutical capsules. Res J Pharmacogn Phytochem. 2024;16(3):159–64.
51. Suleria HA, Barrow CJ, Dunshea FR. Screening and characterization of phenolic compounds and their antioxidant capacity in different fruit peels. Foods. 2020;9(9):1206.
52. Ullah H, Sommella E, Santarcangelo C, D’Avino D, Rossi A, Dacrema M, Minno AD, Di Matteo G, Mannina L, Campiglia P, Magni P. Hydroethanolic extract of Prunus domestica L.: Metabolite profiling and in vitro modulation of molecular mechanisms associated with cardiometabolic diseases. Nutrients. 2022;14(2):340.
53. Wolf J, Göttingerová M, Kaplan J, Kiss T, Venuta R, Nečas T. Determination of the pomological and nutritional properties of selected plum cultivars and minor fruit species. Hortic Sci (Prague). 2020;47(4).
54. Drogoudi P, Pantelidis G. Phenotypic variation and peel contribution to fruit antioxidant contents in European and Japanese plums. Plants. 2022;11(10):1338.
55. Alajil O, Sagar VR, Kaur C, Rudra SG, Sharma RR, Kaushik R, Verma MK, Tomar M, Kumar M, Mekhemar M. Nutritional and phytochemical traits of apricots (Prunus armeniaca L.) for application in nutraceutical and health industry. Foods. 2021;10(6):1344.
56. Lin X, Huang S, Zhang Q, Zhu S, Dong X. Changes in the primary metabolites of ‘Fengtang’ plums during storage detected by widely targeted metabolomics. Foods. 2022;11(18):2830.
57. Moscatello S, Frioni T, Blasi F, Proietti S, Pollini L, Verducci G, Rosati A, Walker RP, Battistelli A, Cossignani L, Famiani F. Changes in absolute contents of compounds affecting the taste and nutritional properties of the flesh of three plum species throughout development. Foods. 2019;8(10):486.
58. Pino JA, Quijano CE. Study of the volatile compounds from plum (Prunus domestica L. cv. Horvin) and estimation of their contribution to the fruit aroma. Food Sci Technol. 2012;32:76–83.
59. Ahire SM, Pawar PS, Sonawane VN, Jadhav SP. Personalized medicine and pharmacogenomics: Impact of genetic variation on drug response and individualized therapy—a review. Asian J Pharm Technol. 2026;16(1):91–8.
60. Alwan AM, Rokaya D, Kathayat G, Afshari JT. Onco-immunity and therapeutic application of amygdalin: A review. J Oral Biol Craniofac Res. 2023;13(2):155–63.
61. Bolarinwa IF, Orfila C, Morgan MR. Amygdalin content of seeds, kernels and food products commercially available in the UK. Food Chem. 2014;152:133–9.
62. Hasanabadi PS, Shaki F. The pharmacological and toxicological effects of amygdalin: A review study. Pharm Biomed Res. 2022.
63. Naryal A, Bhardwaj P, Kant A, Chaurasia OP, Stobdan T. Altitude and seed phenotypic effect on amygdalin content in apricot (Prunus armeniaca L.) kernel. Pharmacogn J. 2019;11:332–7.
64. Savic IM, Savic Gajic IM. Determination of physico-chemical and functional properties of plum seed cakes for estimation of their further industrial applications. Sustainability. 2022; 14(19):12601.
65. Zaynab M, Fatima M, Abbas S, Sharif Y, Umair M, Zafar MH, Bahadar K. Role of secondary metabolites in plant defense against pathogens. Microb Pathog. 2018; 124: 198–202.
66. Zhang H, Tsao R. Dietary polyphenols, oxidative stress and antioxidant and anti-inflammatory effects. Curr Opin Food Sci. 2016; 8: 33–42.
67. Monjotin N, Amiot MJ, Fleurentin J, Morel JM, Raynal S. Clinical evidence of the benefits of phytonutrients in human healthcare. Nutrients. 2022; 14(9): 1712.
68. Caesar LK, Cech NB. Synergy and antagonism in natural product extracts: When 1 + 1 does not equal 2. Nat Prod Rep. 2019; 36(6): 869–88.
69. Mishra S, Vyas S. Therapeutic and pharmacological potential of Prunus domestica: A comprehensive review. Int J Pharm Sci Res. 2021; 12: 3034–41.
70. Kovacikova E, Kovacik A, Halenar M, Tokarova K, Chrastinova L, Ondruska L, Jurcik R, Kolesar E, Valuch J, Kolesarova A. Potential toxicity of cyanogenic glycoside amygdalin and bitter apricot seed in rabbits—health status evaluation. J Anim Physiol Anim Nutr. 2019;103(2):695–703.
71. Wani SM, Jan N, Wani TA, Ahmad M, Masoodi FA, Gani A. Optimization of antioxidant activity and total polyphenols of dried apricot fruit extracts (Prunus armeniaca L.) using response surface methodology. J Saudi Soc Agric Sci. 2017;16(2):119–26.
72. Fatima T, Bashir O, Gani G, Bhat T, Jan N. Nutritional and health benefits of apricots. Int J Unani Integr Med. 2018;2(2):5–9.
73. Al-Soufi MH, Alshwyeh HA, Alqahtani H, Al-Zuwaid SK, Al-Ahmed FO, Al-Abdulaziz FT, Raed D, Hellal K, Mohd Nani NH, Zubaidi SN, Asni NS. A review with updated perspectives on nutritional and therapeutic benefits of apricot and the industrial application of its underutilized parts.Molecules.2022;27(15): 5016.
74. Askarpour M, Ghalandari H, Setayesh L, Ghaedi E. Plum supplementation and lipid profile: A systematic review and meta-analysis of randomized controlled trials. J Nutr Sci. 2023; 12: e6.
75. Mullins A, Akhavan N, Arjmandi B, Ormsbee L. Study protocol: Effects of daily prune consumption on lipid profile, inflammation, and oxidative stress. Curr Dev Nutr. 2022;6:1150.
76. Jadhav SP, Ahire SM, Pawar PS, Mahajan SK, Sonawane DD. Exploring natural oils: Role in antimicrobial activity and preservation. Asian J Res Pharm Sci. 2026; 16(1): 59–64.
77. Buskaran K, Bullo S, Hussein MZ, Masarudin MJ, Mohd Moklas MA, Fakurazi S. Anticancer molecular mechanism of protocatechuic acid loaded on folate-coated functionalized graphene oxide nanocomposite delivery system in human hepatocellular carcinoma. Materials. 2021; 14(4): 817.
78. El-Beltagi HS, El-Ansary AE, Mostafa MA, Kamel TA, Safwat G. Evaluation of the phytochemical, antioxidant, antibacterial and anticancer activity of Prunus domestica fruit. Not Bot Horti Agrobot Cluj Napoca. 2019; 47(2): 395–404.
79. Bahrin AA, Moshawih S, Dhaliwal JS, Kanakal MM, Khan A, Lee KS, Goh BH, Goh HP, Kifli N, Ming LC. Cancer protective effects of plums: A systematic review. Biomed Pharmacother. 2022; 146: 112568.
80. Hooshmand S, Kern M, Metti D, Shamloufard P, Chai SC, Johnson SA, Payton ME, Arjmandi BH. The effect of two doses of dried plum on bone density and bone biomarkers in osteopenic postmenopausal women: A randomized controlled trial. Osteoporos Int. 2016; 27(7): 2271–9.
81. Wallace TC. Dried plums, prunes and bone health: A comprehensive review. Nutrients. 2017; 9(4): 401.
82. Silvan JM, Michalska-Ciechanowska A, Martinez-Rodriguez AJ. Modulation of antibacterial, antioxidant, and anti-inflammatory properties by drying of Prunus domestica L. plum juice extracts. Microorganisms. 2020; 8(1):119.
83. Siddiqui SA, Anwar S, Yunusa BM, Nayik GA, Khaneghah AM. The potential of apricot seed and oil as functional food: Composition, biological properties, health benefits and safety. Food Biosci. 2023; 51: 102336.
84. Lever E, Scott SM, Louis P, Emery PW, Whelan K. The effect of prunes on stool output, gut transit time and gastrointestinal microbiota: A randomized controlled trial. Clin Nutr. 2019;38(1):165–73.
85. Simpson AM, De Souza MJ, Damani J, Rogers C, Williams NI, Weaver C, Ferruzzi MG, Chadwick-Corbin S, Nakatsu CH. Prune supplementation for 12 months alters the gut microbiome in postmenopausal women. Food Funct. 2022; 13(23): 12316–29.
86. Alasalvar C, Chang SK, Kris-Etherton PM, Sullivan VK, Petersen KS, Guasch-Ferré M, Jenkins DJ. Dried fruits: Bioactives, effects on gut microbiota, and possible health benefits—an update. Nutrients. 2023; 15(7): 1611.
87. Mihaylova D, Popova A, Alexieva I, Krastanov A, Lante A. Polyphenols as suitable control for obesity and diabetes. Open Biotechnol J. 2018; 12: 219–28.
88. Lankatillake C, Luo S, Flavel M, Lenon GB, Gill H, Huynh T, Dias DA. Screening natural product extracts for potential enzyme inhibitors: Protocols and standardization of the usage of blanks in α-amylase, α-glucosidase and lipase assays. Plant Methods. 2021; 17(1): 3.
89. Magiera A, Kołodziejczyk-Czepas J, Skrobacz K, Czerwińska ME, Rutkowska M, Prokop A, Michel P, Olszewska MA. Valorisation of the inhibitory potential of fresh and dried fruit extracts of Prunus spinosa L. towards carbohydrate hydrolysing enzymes, protein glycation, multiple oxidants and oxidative stress-induced changes in human plasma constituents. Pharmaceuticals. 2022; 15(10): 1300.
90. Marčetić M, Samardžić S, Ilić T, Božić DD, Vidović B. Phenolic composition, antioxidant, anti-enzymatic, antimicrobial and prebiotic properties of Prunus spinosa L. fruits. Foods. 2022; 11(20): 3289.
91. Vahedi-Mazdabadi Y, Karimpour-Razkenari E, Akbarzadeh T, Lotfian H, Toushih M, Roshanravan N, Saeedi M, Ostadrahimi A. Anti-cholinesterase and neuroprotective activities of sweet and bitter apricot kernels (Prunus armeniaca L.). Iran J Pharm Res. 2020; 19(4): 216.
92. Ahire SM, Jadhav SP, Sonawane VN, Shewale VV, Pawar PS, Chavan DB, Mahaparale SP, Mahajan SK. A comprehensive review on formulation and evaluation of herbal niosomes containing Phaseolus vulgaris and Zingiber officinale for the treatment of diabetes mellitus. Int J Adv Multidiscip Res Stud. 2024; 4(6): 710.
93. Joshi VK, Gill A, Kumar V, Chauhan A. Preparation of plum wine with reduced alcohol content: Effect of must treatment and blending with sand pear juice on physico-chemical and sensory quality. Indian J Nat Prod Resour. 2014; 5(1): 67–74.
94. Jarvis N, O'Bryan CA, Ricke SC, Crandall PG. The functionality of plum ingredients in meat products: A review. Meat Sci. 2015; 102: 41–8.
95. Mohammadi-Moghaddam T, Firoozzare A, Kariminejad M, Sorahi M, Tavakoli Z. Black plum peel as a useful by-product for the production of new foods: Chemical, textural, and sensory characteristics of Halva Masghati. Int J Food Prop. 2020; 23(1): 2005–19.
96. Sorour MA, Mehanni AH, Hussien SM, Mustafa Hassan MA. Chemical composition and functional properties of some fruit seed kernel flours. J Sohag Agrisci. 2021; 6(2): 184–91.
97. Pawar PS, Ahire SM, Shewale VV, Jadhav S, Mahajan SK, Sonawane DD. Silver nanoparticles: A comprehensive review on synthesis, properties and applications. Res J Pharm Dosage Forms Technol. 2025; 17(4): 279–85.
98. Li Y, Tang B, Chen J, Lai P. Microencapsulation of plum (Prunus salicina Lindl.) phenolics by spray drying technology and storage stability. Food Sci Technol. 2017; 38(3): 530–6.
99. Nizioł-Łukaszewska Z. Extracts of cherry and sweet cherry fruit as active ingredients of body wash formulations. Not Bot Horti Agrobot Cluj Napoca. 2019; 47(1): 100–7.
100.Pham TT, Nguyen LL, Dam MS, Baranyai L. Application of edible coating in extension of fruit shelf life. Agri Engineering. 2023; 5(1): 520–36.
101.Stryjecka M, Kiełtyka-Dadasiewicz A, Michalak M, Rachoń L, Głowacka A. Chemical composition and antioxidant properties of oils from the seeds of five apricot (Prunus armeniaca L.) cultivars. J Oleo Sci. 2019; 68(8): 729–38.
102.Nafis A, Kasrati A, Jamali CA, Custódio L, Vitalini S, Iriti M, Hassani L. A comparative study of the in vitro antimicrobial and synergistic effect of essential oils from Laurus nobilis L. and Prunus armeniaca L. from Morocco with antimicrobial drugs: New approach for health promoting products. Antibiotics. 2020; 9(4): 140.
103.Makrygiannis I, Athanasiadis V, Bozinou E, Chatzimitakos T, Makris DP, Lalas SI. An investigation into apricot pulp waste as a source of antioxidant polyphenols and carotenoid pigments. Biomass. 2022; 2(4): 334–47.
104.Mateus AR, Pena A, Sendon R, Almeida C, Nieto GA, Khwaldia K, Silva AS. By-products of dates, cherries, plums and artichokes: A source of valuable bioactive compounds. Trends Food Sci Technol. 2023; 131: 220–43.
105.Mihaylova D, Desseva I, Tumbarski Y, Popova A, Pandova S, Lante A. Evaluation of the enzyme inhibition, antioxidant, and antimicrobial activities of apricots, plums, and their hybrid fruits. Plants. 2024; 13(20): 2936.
106.Mishra S, Tiwari S, Pal SK, Shukla P. Formulation and evaluation of herbal face mask sheet. Int J Pharm Sci. 2024; 2(9): 147–60.
107.Thakur A, Kumar A, Kaya S, Benhiba F, Sharma S, Ganjoo R, Assad H. Electrochemical and computational investigations of Thysanolaena latifolia leaves extract: An eco-benign solution for the corrosion mitigation of mild steel. Results Chem. 2023; 6: 101147.
108.Singh S, Sharma S. Nutraceuticals-based nano-formulations: An overview through clinical validations. In: Advances in Nutraceuticals and Functional Foods. 2022. p. 277–309.
109.Michalak M. Plant-derived antioxidants: Significance in skin health and the ageing process. International Journal of Molecular Sciences. 2022 Jan; 23(2): 585.
110.Ahire SM, Jadhav SP, Shewale VV, Pawar PS, Kokande AM, Sonawane DP, Patil DM. A review on computer-aided drug design and discovery. J Reattach Ther Dev Divers. 2023; 6: 1573–82.
111.Li M, Xiao Y, Mount S, Liu Z. An atlas of genomic resources for studying Rosaceae fruits and ornamentals. Front Plant Sci. 2021; 12: 644881.
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Received on 16.01.2026 Revised on 24.02.2026 Accepted on 28.03.2026 Published on 08.07.2026 Available online from July 13, 2026 Res. J. Pharmacognosy and Phytochem. 2026; 18(3):259-270. DOI: 10.52711/0975-4385.2026.00038 ©A&V Publications All right reserved
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