ISSN : 0970 - 020X, ONLINE ISSN : 2231-5039
     FacebookTwitterLinkedinMendeley

A Review of the Antioxidant and Antimicrobial Activities and Photoprotective Properties of Psidium guajava L.

Darshani Hansamani Dewage Dewage Donaand Chandima Shashikala Kumari Rajapakse*

Department of Chemistry, University of Kelaniya, Kelaniya, Sri Lanka.

Corresponding Author E-mail:shashikala@kln.ac.lk

DOI : http://dx.doi.org/10.13005/ojc/400505

Article Publishing History
Article Received on : 23 Sep 2024
Article Accepted on : 25 Oct 2024
Article Published : 07 Nov 2024
Article Metrics
Article Review Details
Reviewed by: Dr. Shuai Hu
Second Review by: Dr. Noshin
Final Approval by: Dr. Abdelwahab Omri
ABSTRACT:

Psidium guajava L. popularly known as a poor man's apple is not just a tropical plant that provides delicious fruit but also offers numerous benefits for mankind across various disciplines due to its rich pool of phytochemicals with bioactive properties. Many scientific investigations confirmed that guava leaves, fruit pulp, peel, and seeds are rich in compounds with nutritional, pharmacological, medicinal, and cosmeceutical properties. The objective of this comprehensive review is to compile the data on photoprotective properties (ultraviolet protection), antioxidants, and antimicrobial activities of Psidium guajava L. published in the last two decades and to discuss how these properties are advantageous for potential photoprotective cosmeceutical industrial applications.

KEYWORDS:

Antioxidant; Antimicrobial; Psidium guajava L.; Ultraviolet

Download this article as: 

Copy the following to cite this article:

Dona D. H. D. D, Rajapakse C. S. K. A Review of the Antioxidant and Antimicrobial Activities and Photoprotective Properties of Psidium guajava L. Orient J Chem 2024;40(5).


Copy the following to cite this URL:

Dona D. H. D. D, Rajapakse C. S. K. A Review of the Antioxidant and Antimicrobial Activities and Photoprotective Properties of Psidium guajava L. Orient J Chem 2024;40(5). Available from: https://bit.ly/4hFl22U


Introduction

Guava, scientifically known as Psidium guajava L. is a small tree of the Myrtaceae family1. It mostly grows in tropical and subtropical areas in the world2,3. The major phytochemicals of guava are flavonoids, phenols, tannins, terpenes, saponins, alkaloids, glycosides, coumarins, etc4-6 which exhibit varieties of properties that are very useful to human health as herbal medicine, and a cosmeceutical ingredient7,8.

Guava (Psidium guajava L.) stands as a year-round fruit tree with antioxidant-rich fruits9. Its fruit, leaves, and seeds have garnered attention due to their substantial antioxidant potential10,11, attributed to their robust polyphenolic and flavonoid contents12. Guava boasts a repertoire of food and nutritional values along with potent bioactive properties, including antioxidative7,9,13, antidiabetic14,15, antimicrobial16-18, anti-inflammatory14,20, anticancer20,21, anti-diarrheal22,23, antimutagenic24,25, hepatoprotective26,27, anti-hemolytic28,29, antimalarial30,31, antitussive32,33, antigenotoxic34,35, wound healing36,37 and cardiovascular protective effects 38,39.

Guava is known to be rich in a diverse range of phytochemicals, including alkaloids, steroids, flavonoids, quinones, oils, fats, phenolics, starch, tannins, terpenoids, glycosides, saponins, vitamin C, carotenoids, and more40-42. Lutein and zeaxanthin protect the retina from UV-induced oxidative damage. Polyphenols also demonstrate photoprotective effects43,44. One standout example is Epigallocatechin-3-gallate (ECGC), a polyphenol that effectively combats UV-associated maladies45. Studies have shown that guava fruits are rich in bioactive compounds, particularly ellagic acid, kaempferol glycosides, quercetin derivatives, catechins, and proanthocyanidins46-51. These compounds contribute to the fruit’s antioxidant properties. Additionally, guava fruits contain citric acid, oleanolic acid, and various anthocyanidins9,42. The leaves are also a valuable source of phytochemicals, including essential oils like carvone, fatty acids, and terpenoids such as β-caryophyllene, eugenol, and α-copaene20. Furthermore, guava leaves contain flavonoids, phenolic acids, and other antioxidants, such as gallic acid, rutin, and ferulic acid19. The peel is particularly abundant in ellagic acid, tannins, triterpenoids, and flavonols, enhancing its health benefits18.

The awareness of the potential risks associated with continuous sun exposure has led to a significant increase in the use of sunscreen creams over the past few decades52. As people become more informed about the harmful effects of UV radiation, especially UV-B and UV-A, they seek protective measures to mitigate these risks53. Sunscreens, specifically designed to shield the skin from the adverse effects of UV radiation, have become a vital societal awareness in skin protection 54. While visible light (with wavelengths ranging from 400 to 740 nm) and infrared radiation (wavelengths above 760 nm) affect the skin55, UV radiation poses the most immediate and significant threat to skin health. The harmful impact of UV radiation, including sunburn, photoaging, and an increased risk of skin cancer, underscores the importance of effective sun protection measures56,57.

In light of these concerns, there is an ongoing effort to develop herbal-based sunscreens that offer effective UV protection while minimizing potential adverse effects on the skin58. This has led to an increased interest in exploring natural sources of photoprotective compounds, such as those found in plant and fruit extracts, which may provide a safer and more sustainable alternative for sun protection cosmetics59. Indeed, the use of natural bioactive substances in sun protection cosmetics has gained significant attention due to their potential to provide effective photoprotection while offering additional benefits for the skin’s overall health and appearance60. Natural compounds often possess a range of bioactivities, including antioxidant, antimicrobial, and anti-aging properties. These properties can work synergistically to counteract the adverse effects of UV radiation and promote healthier skin61,62.

Many herbal cosmeceuticals incorporate a range of natural components, each contributing to the overall benefits of the product63. One notable advantage is the presence of natural antioxidants and other secondary metabolites, which bring nutritional and antimicrobial properties to the formulation64. Additionally, these products often contain vitamins that provide supplementary protection to the skin. Importantly, this combination of elements contributes to achieving enhanced skin protection while minimizing potential side effects, a characteristic that stands in contrast to synthetic cosmetic products65.

Furthermore, the antimicrobial properties of certain natural compounds can help protect the skin from harmful microorganisms that may thrive under UV exposure66. This can contribute to maintaining the skin’s health and integrity, preventing potential infections or irritations caused by microbial activity67. Additionally, the anti-aging properties of some natural compounds can aid in maintaining the skin’s youthful appearance and minimizing the effects of UV-induced aging68. These compounds can support collagen production, skin elasticity, and overall skin health, helping mitigate the negative impact of long-term sun exposure 69. Given the potential benefits of natural bioactive substances, the cosmeceutical industry has been increasingly incorporating herbal products into sunscreen formulations70. Many cosmeceutical products now include one or more natural agents as active ingredients alongside primary sun protection components71. This approach aims to offer consumers effective sun protection and the potential for improved skin health and appearance.

In the field of phytocosmetics, plant extracts with antioxidant potential are of significant interest since they include compounds that might neutralize reactive oxygen species, improve skin homeostasis, and avoid erythema and premature skin aging72. Nowadays, a wide variety of extracts of plant species are included in sunscreen formulations73. These include extracts of Aloe-vera (Aloe barbadensis miller), lemon (Citrus limon L.), cucumber (Cucumus sativus L.), green tea (Camellia sinensis), Eastern prickly pear cactus (Opuntia humifusa), African tulip tree (Spathodea campanulata L.), tomatoes (Solanum lycopersicum), Indian beech tree (Pongamia pinnata L.), Dendropanax morbifera and pomegranate (Punica granatum)74. They serve as biological agents in sun protection cosmetics by moisturizing, preserving, smoothing, and emulsifying for skin protection75.

Data Collection and Analysis

A comprehensive literature search was undertaken using search engines and databases including Sci-finder, Google Scholar, Research Gate, PubMed, and Science Direct to locate publications discussing the bioactivities of Psidium guajava L. that are important for the development of sunscreens using Guava extracts. The keywords used for the relevant literature search were antioxidant, antimicrobial, cosmeceuticals, Psidium guajava L. and ultraviolet. These keywords were chosen due to the plant material (Psidium guajava L.), and properties (antioxidant, antimicrobial, and photoprotective) that give significant contributions to the scope, and the search was done individually and using keywords as a combination. This review extensively encompasses findings from a total of 101 research papers, spanning from last two decades. Even though the keyword search gave 3,070 articles, only those published in English and relevant to the scope of this review were considered.

Antioxidant properties of Guava

Guava, which has a unique collection of phytochemicals, has attracted attention as a potent anti-aging agent with strong antioxidant effects to be used as a cosmeceutical ingredient76. They reduce oxidative skin damage by preventing the generation of reactive oxygen species induced by external (UV radiations) and endogenous factors77. The antioxidant potential of the different plant parts of the Psidium guajava is summarized in Table 1. It further summarizes the methods used to extract the chemical constituents from different plant parts and the antioxidant assays conducted to determine their antioxidant activities. The assays that have been used to determine the antioxidant activity of the plant parts include, 2,2-Diphenyl-1-picrylhydrazyl (DPPH), 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid (ABTS+), Ferric ion reducing antioxidant power (FRAP), thiobarbituric acid (TBA) and Ferric Thiocyanate (FTC).

Table 1: Antioxidant activities of guava plant parts

Plant part

Solvent/s used for extraction          

Type of assay

Results

References

Leaves

The material was submerged in 70% ethyl alcohol and then subjected to boiling in a water bath at 100 °C for 10 minutes

DPPH, ABTS+

The DPPH assay yielded a comparable result (444.05 ± 1.01 mg TE/g extract) to the outcome obtained in the ABTS assay (424.80 ± 31.05 mg TE/g extract)

50

Leaves

Soxhlet extraction was performed using methanol and hexane as solvents

DPPH, nitric oxide radical-scavenging activity and superoxide radical-scavenging activity

In comparison to the methanolic extract, the hexane extract from Psidium guajava L. leaves exhibited reduced effectiveness in scavenging oxidation, as indicated by diminished activity against 1,1-diphenyl-2-picrylhydrazyl (DPPH), nitric oxide, superoxide, and α-glucosidase inhibitory activity

28

Leaves

The guava leaves were boiled with distilled water, followed by filtration. Subsequent extractions using ethanol and methanol were carried out through maceration.

DPPH, ABTS+, Reducing power assay, nitric oxide radical-scavenging activity and nitrite-scavenging activity

The guava leaves exhibited higher scavenging activity against DPPH and ABTS•+ radicals, as well as stronger reducing power in the water extract compared to pure ethanol and methanol extracts

78

Leaves

Essential oil (EO) from guava leaves was re-dissolved in methanol (MeOH)

DPPH

Exhibited a moderate antioxidant effect, with an IC50 value of 460.37 ± 1.33 μg/mL

79

Leaves

Macerated into 95% ethanol

DPPH

The IC50 value was determined to be 53.2 μg/ml

80

Leaves

Sonication (E1), Soxhlet extraction (E2), agitated maceration (E3), and heated agitated maceration (E4)

FRAP, DPPH

The extraction method E4 exhibited the highest total antioxidant capacity (432.57 ± 0.51 mg Trolox Eq/g), while the DPPH radical scavenging assay demonstrated the lowest IC50 value in E3 (273.81 ± 0.07 ppm)

4

Fruit

The pretreated sample was extracted using methanol that was acidified with concentrated hydrochloric acid

DPPH and

ABTS+

The antioxidant activity obtained from DPPH assay and ABTS assay in values of 5.22–5.62 TEAC 100 g−1 dried weight and 17.63–18.74 TEAC 100 g−1 dried weight, respectively

47

Fruit

Macerated using 80% methanol (80:20 methanol-water,

v/v, 200 ml)

DPPH

The DPPH inhibition percentage ranges from 36.8% to 71% across different guava cultivars

81

Peel

Macerated into water

DPPH, FRAP, TBA Assay, FTC assay

The reduction in DPPH radicals followed the sequence: guava peel > Butylated hydroxyanisole (BHA)/Butylated hydroxytoluene (BHT) > ascorbic acid. At a concentration of 200 ppm, the reductive potential of the samples decreased in the order: ascorbic acid (Abs=4.9803) > BHA/BHT (Abs=1.5050) > guava peel (Abs=1.0120). In the TBA assay, guava peel exhibited higher absorbance compared to BHA/BHT and ascorbic acid. As determined by the FTC assay, the antioxidant activity of guava peel extract was measured at 58.91%.

82

Peel, pulp and seed

The material was ground in a mortar following the addition of distilled water (1:9 w/v), then centrifuged. The resulting supernatant was collected and utilized

FRAP

Guava exhibits robust antioxidant activity in both fruit peel and seed fractions

83

Peel, pulp and leaves

Cold extracted into methanol

DPPH

The guava leaf extract displayed the most substantial DPPH activity with an IC50 value of 89.56 ± 0.97 µg/mL, whereas the pulp extract exhibited the lowest antioxidant potential with an IC50 of 119.72 ± 0.55 µg/mL

84

Co-products (discarded fruit material) from the processing of guava

The dry co-product was stirred with ethanol, followed by centrifugation to obtain the supernatant, which was then filtered with ethanol and subsequently diluted

DPPH, FRAP and β-carotene/

linoleic acid system

The guava co-products exhibited antioxidant activity comparable to BHT (butylated hydroxytoluene) at a concentration of 20 µg/mL

85

Moreno et al., (2014) investigated that not only the guava fresh fruit but also the flour obtained from acetonic guava fruit has a considerable amount of antioxidant potential by analyzing the ethanolic, and aqueous extracts of fresh guava juice, fresh guava fruit, and its flour using an improved ABTS method17. This study revealed that all the extracts of guava fruit flour have a higher potential for antioxidant activity than fresh fruit and juice. According to Milani et al. (2018) antioxidant properties of extract of guava waste which is generated in agricultural industries are higher than the standard ellagic acid46. These findings proved that not only the original plant materials but also its waste in agricultural industries have sufficient antioxidant properties. Araújo et al. (2014) discovered that the co-product (discarded fruit material in industry) of guava has high antioxidant activity compared to the standard BHT85.

A study by Shabbir et al., (2020) revealed that the highest DPPH scavenging activity was found in guava pulp methanolic extract than in guava leaf and seed methanolic extracts14. They suggested that because guava pulp contains Vitamin C, it may be the reason for the higher DPPH scavenging activity. According to the study conducted by Yousaf et al., (2020), the antioxidant activity of guava fruits varies in different indigenous guava cultivars81. Guo et al., (2003) showed that guava exhibits robust antioxidant activity in fruit, peel, and seed fractions and their antioxidant activities were determined by the FRAP assay83. Marina and Noriham (2014) reported the antioxidant activity of guava peel extract by using DPPH, FRAP, TBA, and FTC assays82. Research conducted by Liu et al., (2018) found that compared to guava fruit and seed ethanol aqueous extracts, guava peel extract shows significant antioxidant potential compared to other samples in both DPPH, ABTS+, and FRAP assays18. The studies conducted by researchers showed that guava leaves are a great source for phytochemicals with antioxidant properties4,28,50,78-80,84.

Antimicrobial activity of Guava

Guava emerges as a promising candidate, brimming with the source of robust antibacterial agents2,19,84. Investigations have unveiled the antibacterial prowess inherent in various components of the guava plant, including its leaves, fruits, and peels, displaying efficacy against both Gram-positive and Gram-negative bacterial strains86,87. Growther and Sukirtha (2018) evaluated the antimicrobial activity of petroleum ether, benzene, chloroform, ethanol, and methanol extracts of guava bark and leaves against Staphylococcus aureus, Klebsiella pneumoniae, Salmonella typhi, Shigella dysenteriae, Escherichia coli, Pseudomonas aeruginosa and Candida albicans using the agar well diffusion method7. This study showed that both guava leaf methanol extract and bark ethanol extract have significant antimicrobial activity against the tested bacterial and fungal strains.

According to Birdi et al., (2010) Psidium guajava leaves from different areas were used to prepare a decoction extract, which inhibited two bacterial strains including Shigella flexneri (EC50 = 0.98% ± 0.2%) and Vibrio cholerae (EC50 = 2.88% ± 0.36%)22. Another study by Biswas et al., (2013) reported that leaf methanolic and ethanolic extracts of guava showed the highest inhibition activity against Bacillus cereus (8.27 mm and 6.11 mm were the respective mean inhibition zones) and Staphylococcus aureus (12.3 mm and 11.0 mm were the respective mean inhibition zones) which are foodborne and spoilage gram-positive bacteria86. However, the guava leaf extracts didn’t show any antimicrobial effect against gram-negative bacterial organisms. In this study solvents, n-hexane, methanol, ethanol, and boiling distilled water were used as the extraction solvents and the well-diffusion method against Escherichia coli and Salmonella enteritidis which represent gram-negative bacteria and Staphylococcus aureus and Bacillus cereus which represent gram-positive bacteria were used.

Abdelmalek et al., (2016) reported that peel aqueous extract of Psidium guajava L. could be used as a natural preservative due to its high antibacterial activity. An aqueous extract of the peel at a concentration of 10% or higher was effective against coagulase-positive Staphylococcus aureus and methicillin-resistant Staphylococcus aureus (MRSA), while a concentration of 1% or higher was effective against coagulase-negative staphylococci19.  This study showed that guava fruit is not only rich in nutrients but also has good antimicrobial potential in its peel. Das & Goswami (2019) investigated that guava leaf methanolic extract has a significant inhibition against Bacillus subtilis, Saccharomyces cerevisiae, and Aspergillus niger2. However, it showed very little inhibition against Escherichia coli. In this study, they determined the antimicrobial effect of the guava leaf extract against gram-positive (Bacillus subtilis), gram-negative bacteria (Escherichia coli), yeast fungal strain (Saccharomyces cerevisiae), and mold fungal strain (Aspergillus niger).

Ekeleme et al., (2017) determined the antibacterial activity of ethanolic, methanolic, and aqueous crude extracts using Cup-plate agar diffusion bioassay against Pseudomonas aeruginosa, Escherichia coli, Staphylococcus aureus, Streptococcus pneumoniae and Klebsiella pneumoniae88. They found that the guava leaf ethanol extract exhibited antibacterial activity against all isolates except Staphylococcus aureus while the aqueous extract of the leaves displayed a notable level of activity against all tested bacterial isolates at a concentration of 100 mg/L. In the methanol extract, the highest inhibitory activity was observed against Klebsiella pneumonia.

According to Dewage et al., (2023) guava peel and pulp methanolic extracts displayed enhanced antibacterial activity against Staphylococcus aureus and Escherichia coli84. Notably, Pseudomonas aeruginosa exhibited heightened susceptibility to the antibacterial effects of guava pulp extract. Guava peel extract showcased the highest antifungal activity with an inhibition zone of 16.00 ± 2.62 mm, whereas guava pulp showed no antifungal activity. Guava leaves exhibited a moderate level of antimicrobial activity. In this study, they used the agar well diffusion method for methanolic extract of guava peel, pulp and leaves against Escherichia coli (ATCC 25922), Staphylococcus aureus (ATCC 25923), Pseudomonas aeruginosa (ATCC 9027) and Candida albicans (ATCC 10231).

Photoprotective property (UV protection) of Guava

Ultra violet spectrum which ranges from 100 – 400 nm has been divided into 3 different regions. Ultraviolet A region is between 320-400 nanometers while ultraviolet B and ultraviolet C are between 280-320 and 100-280 nanometers, respectively89. UV A and UV B radiations are considered as one of the main reasons behind skin damage leading to sunburn.  UV C is the major biologically damaging radiation to the skin but the ozone layer filters out UV C radiation. Sunscreen ingredients can act as either a physical or a chemical barrier to solar radiation and scatter, absorb, or reflect harmful rays to protect the human skin90.

Melanin, serving as a natural absorber of UV radiation, serves as the body’s initial barrier against the deleterious impacts of UV-induced photodamage. However, there are instances where the melanin levels may fall short of providing adequate protection for the skin91. Various strategies are employed to shield the skin from the adverse consequences of UV exposure, including minimizing sun exposure during peak UV radiation periods, wearing protective clothing, wide-brimmed hats, and sunglasses, as well as the application of sunscreens92. Within sunscreen formulations, the constituents possess the capability to either deflect or absorb ultraviolet rays at the skin’s surface, effectively safeguarding the skin from the detrimental effects of the sun’s UV rays74.

The effectiveness of sunscreen is conventionally measured using the sun protection factor (SPF). The SPF scale categorizes protection levels as follows: Low (SPF 2-15), Medium (SPF 15-30), High (SPF 30-50), and Highest (SPF >50)57. With substantial antimicrobial and antioxidant properties observed in guava (Psidium guajava) fruit and leaves, extensive attention has been directed toward exploring their potential as photoprotective agents for sunscreen in recent years93. In a study conducted by Milani et al., (2018), it was found that extracts from byproducts of guava fruit processing can enhance the effectiveness of chemical UV solar filters46. The research group further illustrated that the phytocosmetic formulation not only absorbed solar radiation within the UV B wavelength range but also significantly enhanced photoprotection efficacy by 17.99% in cosmetic formulations, resulting in an SPF value of 22.3 ± 1.1, surpassing the reference formulation with an SPF value of 18.4 ± 0.7.

Based on research conducted by Ilomuanya et al., (2018) a polyherbal face cream formulation that incorporated extracts of both Psidium guajava leaves and Ocimum gratissimum leaves demonstrated significant antioxidant potential94. This formulation holds the potential to offer preventive benefits against skin carcinogenesis, sunburn, and aging caused by harmful UV rays. The cream’s observed high antioxidant activity is anticipated to yield positive effects on various aspects of skin health, including prevention of aging, sun protection, and potentially even skin cancer prevention. Research conducted by Samejima and Park (2019) demonstrated a substantial level of anti-collagenase activity within the guava leaf’s butanol (BuOH) fraction, surpassing the activity found in other fractions, including the crude extract95. These findings suggest that the leaf extract holds the potential to counteract the processes of skin wrinkling and aging by offering protection against the effects of exposure to ultraviolet radiation.

In a study by Puspaningtyas (2012) it was found that red guava fruit extract possesses tyrosinase enzyme inhibition activity, leading to a reduction in melanin production96. Tyrosinase is a pivotal enzyme in melanin biosynthesis. The inhibition of this enzyme can consequently contribute to the reduction of hyperpigmentation and enhance the skin’s brightness by mitigating melanogenesis. Mota et al., (2019) reported that the SPF value of a sunscreen formulation containing 7.5% 2-ethyl-hexyl methoxycinnamate was significantly improved by approximately 134% when it was incorporated with guava fruit extract97. Dewage et al., (2023) investigated the photoprotective capacity of guava peel, pulp, and leaf methanol extracts84. The study revealed that guava leaf methanolic extract exhibited a notably higher level of photoprotection (SPF = 30.38 ± 0.22) against UV-B radiation in comparison to guava peel (SPF = 20.59 ± 0.49) and pulp (SPF = 16.24 ± 0.67) methanol extracts. Imam et al., (2015) found that a cream developed by using a combination of Psidium gujava, Pyrus communis, and Musa accuminata fruit extracts can block the ultraviolet rays at around 73%61.

Challenges and potentials of Guava extract as an additive in sunscreen formulations

Based on the findings of the studies mentioned, it is evident that guava extracts exhibit significant promise as a natural source in the development of sunscreen products, as leaves and fruits of the plants mainly exhibit antioxidant, antimicrobial as well as photoprotective properties. Scientists discovered and identified many bioactive phenolic and flavonoid compounds in Guava leaves that are responsible for antioxidant and antimicrobial activities including hyperin, epicatechin, quercetin, gallic acid, kaempferol, catechin, avicularin, apigenin, guaijaverin, chlorogenic acid, myricetin and rutin etc98-100. Most of the studies showed that flavonoids and phenolic constituents could have the potential to act as ultraviolet protectors60. Flavonoids also help in maintaining the regular activity of enzymes in the skin and it will affect the division of epithelial cells in the skin61.

Identifying the precise compounds responsible for the photoprotective potential in guava extracts is a critical research gap. Once these specific compounds are identified, they can be isolated and utilized to produce sunscreen formulations with high SPF values. To establish the safe utilization of guava extracts on an industrial scale, it is imperative to conduct both toxicological and clinical studies. Expanding research on the use of guava extracts as additives has the potential to lead to the development of a variety of value-added cosmetic products, targeting the increased demand for herbal products for skin health 101.

Conclusion

Guava (Psidium guajava L.), a tropical fruit rich in bioactive phytochemicals, stands out as a promising candidate for cosmeceutical production.  Even though it has significant bioactivities, a few studies have been conducted to reveal its potential applications to the world. This comprehensive review delves into the cosmetological potential of various parts of the Psidium guajava plant, including leaves, peel, pulp, and seeds. Our focus centers on recent studies, conducted over the past two decades by researchers across the globe, shedding light on the extraction of chemical constituents in guava plant parts and the antioxidant, antimicrobial, and photoprotective attributes inherent to it. While these findings paint a promising picture, they may not be conclusive enough to integrate guava into commercial sunscreen formulations directly. However, by highlighting the need for toxicological evaluations, stability evaluation, and rigorous clinical trials, the reported findings underscore that guava holds the promise of serving as a secure, cost-effective, natural source of ingredients for the cosmeceutical industry.

Funding Sources

The author(s) received no financial support for the research, authorship, and/or publication of this article.

Conflict of Interest

The author(s) do not have any conflict of interest.

Data Availability Statement

This statement does not apply to this article.

Ethics Statement

This research did not involve human participants, animal subjects, or any material that requires ethical approval.

References

  1. Anand, V.; Manikandan.; Kumar, V.; Kumar, S.; Pushpa.; Hedina, A. Phcog J. 2016, 8(4), 314-320.
    CrossRef
  2. Das, M.; Goswami, S.  IJHSR. 2019, 9(2), 39–45.
    CrossRef
  3. Dolkar, D.; Bakshi, P.; Wali, V. K.; Bhushan, B.; Sharma A. Ind. J. Plant Physiol. 2014, 19, 79–82.
    CrossRef
  4. Kokilananthan, S.; Bulugahapitiya, V. P.; Manawadu, H.; Gangabadage, C. S. TJNPR. 2022, 6(4), 552–557.
  5. Naseer, S.; Hussain, S.; Naeem, N.  Clin. phytosci. 2018, 4, 32.
    CrossRef
  6. Jassal, K.; Kaushal, S. Agric. Res. J. 2019, 56(3), 528-533.
    CrossRef
  7. Growther, L.; Sukirtha, K. Asian J. Pharm. Pharmacol. 2018, 4(3), 318-323.
    CrossRef
  8. Lestari, D. A.; Sulastri, N.; Rajebi, O. AMCR. 2022, 3 (3), 285-289.
    CrossRef
  9. Chiari-Andréo, B. G.; Trovatti, E.; Marto, J.; De Almeida-Cincotto, M. G. J.; Melero, A.; Corrêa, M. A.; Chiavacci, L. A.; Ribeiro, H.; Garrigues, T.; Isaac, V. L. B. Braz. J. Pharm. Sci. 2017, 53(2).
    CrossRef
  10. Vyas, N.; Tailang, M.; Gavatia, N. P. Int. J. Pharmtech. Res. 2010, 2(1), 417-419.
  11. Gaber, N.B.; El-Dahy, S.I.; Shalaby, E.A. Biomass Convers. Biorefin. 2023, 13, 4011–4020.
    CrossRef
  12. García‐villegas, A.; Rojas‐garcía, A.; Villegas‐aguilar, M. D. C.; Fernández‐moreno, P.; Fernández‐ochoa, Á.; Cádiz‐gurrea, M. D. I. L.; Arráez‐román, D.; Segura‐carretero, A. Antioxidants. 2022, 11(2), 1–37. 
    CrossRef
  13. Adhalrao, S. B.; Panmand, D. A.; Jawale, S. S.; Salve, J. R.; Gaikwad, S. D. IJARSCT. 2022, 14(1), 234–239.
  14. Shabbir, H.; Kausar, T.; Noreen, S.; Rehman, H. U.; Hussain, A.; Huang, Q.; Gani, A.; Su, S.; Nawaz, A. Animals. 2020, 10(9), 1714.
    CrossRef
  15. Luo, Y.; Peng, B.; Wei, W.; Tian, X.; Wu, Z. Molecules. 2019, 24(7), 1343.
    CrossRef
  16. Thaipong, K.; Boonprakob, U.; Crosby, K.; Cisneros-Zevallos, L.; Hawkins Byrne, D. J. Food Compost. Anal. 2006, 19(6–7), 669–675.
    CrossRef
  17. Moreno, M. A.; Zampini, I. C.; Costamagna, M.; Sayago, J. E.; Ordoñez, R. M.; Isla, M. I. FNS. 2014, 05(08), 725–732.
    CrossRef
  18. Liu, X.; Yan, X.; Bi, J.; Liu, J.; Zhou, M.; Wu, X.; Chen, Q. Electrophoresis. 2018, 39(13), 1654–1662.
    CrossRef
  19. Abdelmalek, S.; Mohsen, E.; Awwad, A.; Issa, R. IAJAA. 2016, 6(3), 1-9.
  20. Ryu, N. H.; Park, K. R.; Kim, S. M.; Yun, H. M.; Nam, D.; Lee, S. G.; Jang, H. J.; Ahn, K. S.; Kim, S. H.; Shim, B. S.; Choi, S. H.; Mosaddik, A.; Cho, S. K.; Ahn, K. S. J. Med. Food. 2012, 15(3), 231–241.
    CrossRef
  21. Kareem, A. T.; Kadhim, E. J. Plant Sci. Today (Early Access). 2024,11(2), 853-860.
  22. Birdi, T.; Daswani, P.; Brijesh, S.; Tetali, P.; Natu, A.; Antia, N. BMC Complement. Altern. Med. 2010, 10(33).
    CrossRef
  23. Faulinza, E. EHI. 2021, 3(1), 131-135.
    CrossRef
  24. S. T. GJP. 2020, 14(2), 17-27.
  25. Andrade-Vieira, L. F.; Palmieri, M. J.; Botelho, C. M.; Luber, J.; Silva, M. F. F. S. Afr. J. Bot. 2017, 113, 443–448.
    CrossRef
  26. Osman, M.; Ahmed, M.; Mahfouz, S.; Elaby, S. N. Y. Sci. J. 2011, 4(3), 27–39.
  27. Dange, S. S.; Rao, P. S.; Jadhav R. S. World J. Pharm. Res. 2020, 9(5), 452-464.
  28. Aprilia, R.; Purba, P.; Paengkoum, P. Molecules. 2022, 27(24), 89-87.
  29. Thephinlap, C.; Pangjit, K.; Suttajit, M.; Srichairatanakool, S. J. Med. Plant Res. 2013, 7(27), 2001-2009.
  30. Rajendran, C.; Begam, M.; Kumar, D.; Baruah, I.; Gogoi, H. K.; Srivastava, R. B.; Veer, V. J. Parasit. Dis. 2014, 38, 148–152.
    CrossRef
  31. , M.; Abu-Lafi, S.; Abu-Remeleh, Q.; Lutgen, P. Pharm. pharmacol. int. j. 2021, 9(1), 11-15.
    CrossRef
  32. Sekhar, N. C.; Jayasree, T.; Ubedulla, S.; Dixit, R.; Manohar, V. S.; Shankar, J. JCDR. 2014, 8(9), HF01-HF04.
  33. Gupta, G. K.; Chahal, J.; Arora, D. J. Pharm. Res. 2011, 4(1), 42-46.
  34. Cesar, P. H. S.; Trento, M. V. C.; Oliveira, D. A.; Simão, A. A.; Vieira, L. F. A.; Marcussi, S. Nat. Prod. Commun. 2017, 12(6).
    CrossRef
  35. Yahaya, T.; Obaroh, I.; Sifau, M.; Salisu, T.; Musa, M. N.; Abdulgafar, I. B. Pharm. Biomed. Res. 2021, 9(1),17-26.
  36. Delorino, S. B.; Ogalesco, M. L.; Rebadulla, K. R.; Rongcales, M. T. A.; Salubre, V. J. I. A.; Talacay, M. K. S.; Tuballas, Z. B. Journal of Pharmaceutical Research International. 2021, 32(41), 27–35.
    CrossRef
  37. Shetty, P.; Chacko, N.; Alva, A.; Kumar, V.; Kandige, P. S.; Gururaj M. P.; Joshi, H.; D’ souza, U. P. RJPT, 2019, 12(12), 6067-6070.
    CrossRef
  38. Nutr. Metab. 2010, 7(9).
    CrossRef
  39. Hsieh, C. L.; Lin, Y. C.; Yen, G. C.; Chen, H. Y. Food chem. 2007, 103, 528–535.
    CrossRef
  40. Haleem Khan, A. A.; Naseem.; Vardhini, B. V. SpringerBriefs in Applied Sciences and Technology. 2016, 7, 81-89.
    CrossRef
  41. Gayathri, V.; Kiruba, D. IJPPR. 2014, 6(2), 332–334.
  42. Rojas-Garbanzo, C.; Zimmermann, B. F.; Schulze-Kaysers, N.; Schieber, A. Food Res. Int. 2017, 100(3), 445–453.
    CrossRef
  43. Câmara, J. S.; Albuquerque, B. R.; Aguiar, J.; Corrêa, R. C. G.; Gonçalves, J. L.; Granato, D.; Pereira, J. A. M.; Barros, L.; Ferreira, I. C. F. R. Foods. 2021, 10(1), 37.
    CrossRef
  44. , F. G.; Dantas, M. O.; Santos, J. P. M.; Froes, S. S.; Gama, J. P. S.; Boaro, C. S. F. Horticulturae. 2023, 9(12), 1291.
    CrossRef
  45. Anunciato, T. P.; da Rocha Filho, P. A. J. Cosmet. Dermatol. 2012, 11(1), 51–54.
    CrossRef
  46. Milani, L. P. G.; Garcia, N. O. S.; Morais, M. C.; Dias, A. L. S.; Oliveira, N. L.; Conceic, E. C. Rev. Bras. Farmacogn. 2018, 28(6), 692–696.
    CrossRef
  47. Nei, W.; Celeste, M.; Maria, A.; De Andrade, D.; Almeida, R. S.; Caldas, C. Microchem. J. 2017, 133, 583–592.
    CrossRef
  48. Mccook-russell, K. P.; Nair, M. G.; Facey, P. C.; Bowen-forbes, C. S. Food Chem. 2012, 134(2), 1069–1073.
    CrossRef
  49. Edozie, I.; Uloma, O.; Chigozie, F. Afr. cient. rep. 2022, 1(3), 161–173.
  50. Ruksiriwanich, C. W.; Khantham, A.; Muangsanguan, Y.; Phimolsiripol, F. J.; Barba, K.; Sringarm, P.; Rachtanapun, K.; Jantanasakulwong, P.; Jantrawut, C.; Chittasupho, R.; Chutoprapat, K.; Boonpisuttinant.; Sommano, S. R. Plants. 2022, 11(24), 3514.
    CrossRef
  51. Lee, D.; Weon, K. Y.; Nam, J. H.; Kyung, W.; Dong-gu, I. Exp. Dermatol. 2016, 25(12), 977-982.
    CrossRef
  52. Mejía-Giraldo, J. C.; Gallardo, C.; Puertas-Mejía, M. A. Photochemistry and Photobiology, 2022, 98, 211-219.
    CrossRef
  53. D’Orazio, J.; Jarrett, S.; Amaro-Ortiz, A.; Scott, T. Int. J. Mol. Sci. 2013, 14(6), 12222-12248.
    CrossRef
  54. Biniek, K.; Levi, K.; Dauskardt, R. H. PNAS. 2012, 109(42), 17111-17116.
    CrossRef
  55. Tang, X.; Yang, T.; Yu, D.; Xiong, H.; Zhang, S. Environ. Int. 2024, 185, 108535.
    CrossRef
  56. Clin. Cosmet. Investig. Dermatol. 2020, 13, 717–730.
    CrossRef
  57. Geoffrey, K.; Mwangi, A. N.; Maru, S. M. Saudi Pharm J. 2019, 27(7), 1009–1018.
    CrossRef
  58. He, H.; Li, A.; Li, S.; Tang, J.; Li, L.; Xiong, L. Biomed. Pharmacother. 2021, 134.
    CrossRef
  59. Oliveira, A. M. S.; de Souza Batista, D.; de Castro, T.N. Photochem. Photobiol. Sci. 2024, 23(5), 853–869.
    CrossRef
  60. Li, L.; Chong, L.; Huang, T.; Ma, Y.; Li, Y.; Ding, H. Animal model. exp. med. 2023, 6(3), 183-195.
    CrossRef
  61. Imam, S.; Azhar, I.; Mahmood, Z. A. Asian J. Pharm. Clin. Res. 2015, 8(3), 234-237.
  62. Yarnell, E.; Abascal, K. Alternative and Complementary Therapies. 2012, 18(3).
    CrossRef
  63. Radice, M.; Manfredini, S.; Ziosi, P.; Dissette, V.; Buso, P.; Fallacara, A.; Vertuani, S. Fitoterapia. 2016, 114, 144-162.
    CrossRef
  64. Verma, A.; Zanoletti, A.; Kareem, K. Y. Environ. Chem. Lett. 2024, 22, 273–295.
    CrossRef
  65. Siavash, H. C.; Fadzilah, A. A. M. Afr. J. Biotechnol. 2011, 10(65), 4573–14582.
    CrossRef
  66. Souak, D.; Barreau, M.; Courtois, A.; André, V.; Duclairoir Poc, C.; Feuilloley, M. G. J.; Gault, M. Microorganisms. 2021, 9, 936.
    CrossRef
  67. Dunaway, S.; Odin, R.; Zhou, L.; Ji L.; Zhang, Y.; Kadekaro, A. L. Front. Pharmacol. 2018, 9, 392.
    CrossRef
  68. Ghazi, S. Results in Chemistry. 2022, 4, 100428.
    CrossRef
  69. Cefali, L. C.; Ataide, J. A.; Moriel, P.; Foglio, M. A.; Mazzola, P. G. Int. J. Cosmet. Sci. 2016, 38(4), 346–353.
    CrossRef
  70. Rasheed, A.; Shama, S.N.; Mohanalakshmi, S. Orient. Pharm. Exp. Med. 2012, 12, 241–246.
    CrossRef
  71. Mishra, A. K.; Mishra, A.; Chattopadhyay, P. Trop. J. Pharm. Res. 2011, 10(3), 352-360.
    CrossRef
  72. Giradkar, P.; Rode, V. JMPAS, 2021, 10(3), 2920–2923.
    CrossRef
  73. Ng, S. Y.; Eh Suk, V. R.; Gew, L. T. J. Cosmet. Dermatol. 2022, 21(11), 5409-5444.
    CrossRef
  74. Saewan, N.; Jimtaisong, A. J. Appl. Pharm. Sci. 2013, 3(9), 129–141.
  75. Ngoc, L. T. N.; Tran, V. V.; Moon, J. Y.; Chae, M.; Park, D.; Lee, Y. C. Cosmetics. 2019, 6(4), 64.
    CrossRef
  76. Kim, S. Y.; Kim, E. A.; Kim, Y. S.; Yu, S. K.; Choi, C.; Lee, J. S.; Kim, Y. T.; Nah, J. W.; Jeon, Y. J. Int. J. Biol. Macromol. 2016, 91, 804–811.
    CrossRef
  77. Shanbhag, S.; Nayak, A.; Narayan, R.; Nayak, U. Y. Adv. Pharm. Bull. 2019, 7(3), 113–117.
  78. Seo, J.; Lee, S.; Elam, M. L.; Johnson, S. A.; Kang, J.; Arjmandi, B. H. Food sci. nutr. 2014, 2(2), 174-80.
    CrossRef
  79. Lee, W. C.; Mahmud, R.; Pillai, S.; Perumal, S.; Ismail, S. APCBEE Procedia. 2012, 2, 86–91.
    CrossRef
  80. Chuanoi, S.; Weerataweeporn, S.; Managit, C.; Pitiporn, S.; Kamkaen, N. J. Health Res. 2009, 23(4), 163–167.
  81. Yousaf, A. A.; Abbasi, K. S.; Ahmad, A.; Hassan, I.; Sohail, A.; Qayyum, A.; Akram, M. A. FS&T. 2020, 41(1).
    CrossRef
  82. Marina, Z.; Noriham, A. Int. Food Res. J. 2014, 21(5), 1925–1929.
  83. Guo, C.; Yang, J.; Wei, J.; Li, Y.; Xu, J.; Jiang, Y. Nutr. Res. 2003, 23(12), 1719–1726.
    CrossRef
  84. Dewage, D. D. D. H.; Samarakoon, S. M. G. K.; Karunarathne, S. H. S.; Rajapakse, C. S. K. Asian J. Chem. 2023, 35(1), 89–94.
    CrossRef
  85. Araújo, K. L. G. V.; Magnani, M.; Nascimento, J. A.; Souza, A. L.; Epaminondas, P. S.; Souza, A. L.; Queiroz, N.; Souza, A. G. Molecules. 2014, 19(3), 3110–3119.
    CrossRef
  86. Biswas, B.; Rogers, K.; Mclaughlin, F.; Daniels, D.; Yadav, A. Int. J. Microbiol. 2013, 746165.
    CrossRef
  87. Metwally, A. M.; Omar, A. A.; Harraz, F. M.; El Sohafy, S. M. Pharmacogn. Mag. 2010, 6(23), 212-8.
    CrossRef
  88. Ekeleme, K.; Tsaku, P.; Nkene, I.; Ufomadu, U.; Abimiku, R.; Oti, V.; Sidi, M. GSCBPS. 2017, 1(2), 013–019.
    CrossRef
  89. Maddodi, N.; Jayanthy, A.; Setaluri, V. Photochemistry and Photobiology. 2012, 88(5), 1075-1082.
    CrossRef
  90. Morabito, K.; Shapley, N. C.; Steeley, K. G.; Tripathi, A. Int. J. Cosmet. Sci. 2011, 33(5), 385-390.
    CrossRef
  91. Brenner, M.; Hearing, J. V. Photochemistry and Photobiology. 2008, 84(3), 539–549. 
    CrossRef
  92. Kapoor, S.; Saraf, S. Pharmacogn. Mag. 2009, 5(19), 238-248.
  93. Dutra, E. A.; Oliveira, D. A. G. C.; Kedor-Hackmann, E. R. M.; Santoro, M. I. R. M. Braz. J. Pharm. Sci. 2004, 40(3), 381–385.
    CrossRef
  94. Ilomuanya, M. O.; Ajayi, T.; Cardoso-Daodu, I.; Akhimien, T.; Adeyinka, O.; Aghaizu, C. Niger. J. Pharm. Sci. 2018, 14(1), 61-68.
  95. Samejima, H.; Park, B. TAD. 2019, 63,12–17.
    CrossRef
  96. Puspaningtyas, A. R. Int. Curr. Pharm. J. 2012, 1(5), 92–97.
    CrossRef
  97. Mota, M. D.; Costa, R. Y. S.; Guedes, A. A. S.; Silva, L. C. R. C. E.; Chinalia, F. A. J. Photochem. Photobiol.  2019, 201, 111639.
    CrossRef
  98. Kumar, M.; Tomar, M.; Amarowicz, R.; Saurabh, V.; Nair, M. S.; Maheshwari, C.; Sasi, M.; Prajapati, U.; Hasan, M.; Singh, S.; Changan, S.; Prajapat, R. K.; Berwal, M. K.; Satankar, V. Foods. 2021, 10(4), 752.
    CrossRef
  99. Wang, L.; Wu, Y.; Bei, Q.; Shi, K.; Wu, Z. J. Sep. Sci. 2017, 40, 3817–3829.
    CrossRef
  100. Liu, C. W.; Wang, Y. C.; Lu, H. C.; Chiang, W. D. Process Biochem. 2014, 49(10), 1601-1605.
    CrossRef
  101. Hernandeza, D. F.; Cervantesa, E. L.; Luna-Vitalb, D. A.; Mojicaa, L. Crit. Rev. Food Sci. Nutr. 2021, 61(22), 3740–3755.
    CrossRef

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.

About The Author