Pharmacy Reports https://doi. org/10. 51511/pr. ORIGINAL ARTICLE Open Access Photoprotective efficacy and physicochemical stability of sunscreen gel containing Averrhoa bilimbi L. leaf extract Rega Gustiya Wittami. Annisa Maulidia Rahayyu*. Untia Kartika Sari Ramadhani Department of Pharmacy. Faculty of Science. Institut Teknologi Sumatera Corresponding author: Jl Terusan Ryacudu. Way Hui. Jati Agung. South Lampung 35365. Email: annisa. rahayyu@fa. Abstract: Chronic UV-B exposure causes significant skin damage, necessitating effective photoprotective strategies. This study developed and evaluated sunscreen gel formulations containing ethanolic extracts of Averrhoa bilimbi leaves at varying concentrations. Extraction was performed using ultrasonic-assisted extraction (UAE), while sun protection factor (SPF) determination employed the Mansur spectrophotometric method. Four gel formulations were prepared: F0 . %, contro. F1 . 2%), F2 . %), and F3 . % extrac. Physicochemical characterization revealed that all formulations exhibited acceptable organoleptic properties, homogeneity, pH . 5 to 7. , viscosity . ,000 to 50,000 cp. , spreadability . to 7 c. , and adhesiveness (>1 secon. Accelerated stability testing demonstrated stable pH, viscosity, spreadability, and SPF values, although adhesiveness showed statistical variation while remaining within acceptable limits. SPF analysis revealed concentration-dependent photoprotective efficacy: F1 achieved maximum protection, while F2 and F3 demonstrated ultraprotection, with F3 exhibiting the highest SPF value of 36. These findings confirm that increased A. bilimbi extract concentration correlates with enhanced photoprotective activity, establishing the potential of this natural ingredient for sunscreen applications. Keywords: Averrhoa bilimbi, natural sunscreen, sun protection factor, gel formulation, photoprotective activity Introduction IndonesiaAos geographical location along the equatorial belt results in prolonged exposure to solar radiation throughout the year, placing the population at elevated risk for UV-induced skin damage. Among the components of solar radiation. UV-B . to 320 n. is recognized as the primary causative agent of skin cancer due to its direct absorption by cellular DNA, leading to mutagenic molecular modifications. UV-B radiation poses a more severe carcinogenic threat compared to UV-A . to 400 n. , which predominantly contributes to photoaging through indirect generation of reactive oxygen species via photosensitization processes . The incidence of skin cancer in Indonesia has demonstrated a concerning upward trend over the past Epidemiological data indicate approximately 2 to 3 million cases of non-melanoma skin cancer and 132,000 cases of melanoma annually . Skin cancer ranks third among cancers affecting Indonesian women, following cervical and breast cancers, with annual incidence rates ranging from 5. 9% to 7. 8% . These statistics underscore the critical need for effective photoprotective strategies in tropical populations. Copyright A The Author. This article is distributed under a Creative Commons Attribution 4. 0 International License Sunscreen products represent a primary preventive measure against UV-induced skin damage. These topical cosmetic formulations function through three distinct mechanisms: absorption, scattering, or reflection of UV radiation . The photoprotective efficacy of sunscreen products is quantified using the Sun Protection Factor (SPF), which measures the degree of protection against UV-B-induced erythema. Sunscreen formulations incorporating adequate SPF values provide a practical and accessible approach to reducing the risk of acute sunburn and long-term photodamage, including carcinogenesis. Recent research has increasingly focused on natural plant-derived photoprotective agents as alternatives or supplements to synthetic UV filters. This trend is driven by consumer preference for natural products, concerns regarding the safety profile of certain synthetic UV filters, and potential environmental impacts of conventional sunscreen ingredients. Plant extracts rich in polyphenolic compounds, particularly flavonoids and phenolic acids, have demonstrated promising UV-absorbing and antioxidant properties, making them suitable candidates for natural sunscreen 1/ 8 Pharmacy Reports Averrhoa bilimbi L. , commonly known as bilimbi or belimbing wuluh, is a tropical fruit tree belonging to the family Oxalidaceae. The leaves of this plant have been utilized in various topical formulations, including bath soaps, antioxidant creams, and peel-off masks, demonstrating its versatility in cosmetic applications . Phytochemical investigations have revealed that bilimbi leaves contain substantial quantities of bioactive secondary metabolites, including flavonoids, phenolic compounds, and tannins, which possess both antioxidant and potential photoprotective properties. These compounds feature conjugated aromatic systems capable of absorbing UV radiation, suggesting their suitability as natural sunscreen agents. Despite the documented bioactivity of A. bilimbi leaf extracts and their incorporation into various cosmetic formulations, no previous studies have specifically investigated their potential as active ingredients in sunscreen gel formulations. Gel-based delivery systems offer several advantages over other topical dosage forms, including superior skin absorption, non-greasy texture, easy application, and favorable aesthetic properties . The semi-solid nature of gels provides both the spreadability of lotions and the substantivity of creams, making them particularly suitable for sunscreen applications where uniform skin coverage is essential. Given the established presence of UV-absorbing phytochemicals in A. bilimbi leaves and the absence of prior research on gel-based sunscreen formulations from this plant material, the present study was designed to address this knowledge gap. The primary objectives of this investigation were: . to formulate sunscreen gel preparations incorporating varying concentrations of A. bilimbi ethanolic leaf extract, . to evaluate the physicochemical properties and stability of the developed formulations, and . to determine their photoprotective efficacy through SPF value assessment. The findings of this study are expected to contribute to the development of effective, plant-based sunscreen products and expand the cosmetic applications of A. bilimbi leaf extracts. This research employed ultrasonic-assisted extraction (UAE) to obtain ethanolic extracts of A. leaves, which were subsequently incorporated into gel formulations at concentrations of 0. 2%, 1%, and 5%, alongside a control formulation without extract. The physicochemical characterization encompassed organoleptic evaluation, homogeneity, pH, viscosity, spreadability, and adhesiveness testing. Accelerated Pharmacy Reports 5. :110 | https://doi. org/10. 51511/pr. bilimbi sunscreen, efficacy and stability stability assessment was conducted using cycling test methodology, and photoprotective efficacy was determined using the spectrophotometric Mansur method for SPF calculation. Through this approach, the study aimed to establish the feasibility and optimize the composition of natural sunscreen gels derived from A. bilimbi leaf extracts. Methods Plant material collection and authentication Fresh mature leaves of Averrhoa bilimbi L. collected from Jalan Bangau Perum BW. Way Huwi Village. Jati Agung District. South Lampung Regency. Lampung Province. Indonesia. Plant authentication was performed at the Botany Laboratory. Department of Biology. Faculty of Mathematics and Natural Sciences. University of Lampung, to confirm the botanical identity and prevent contamination with other species. The specimen was identified as Averrhoa bilimbi L. amily Oxalidacea. Preparation of dried leaf powder The fresh leaves . 53 k. were subjected to wet sorting, washed thoroughly with tap water, and dried under direct sunlight until completely dry, indicated by a crisp texture when crushed. After dry sorting, the dried leaves were ground using a blender and sieved to obtain a fine powder . Moisture content of the powder was determined using a moisture analyzer and maintained below 10% as required by standard herbal processing The simplicia yield was calculated using the formula: . eight of dried simplicia / weight of fresh leave. y 100%. Extraction procedure Ethanolic extraction was performed using the ultrasonic assisted extraction method following the procedure described by Andriani et al. Briefly, 50 g of dried leaf powder was weighed using a digital balance, transferred into a glass beaker, and dissolved in 500 mL of 70% ethanol. The mixture was subjected to ultrasonic extraction at 40AC for 20 The resulting solution was filtered, and the filtrate was concentrated using a rotary evaporator at 40AC and 100 rpm. The concentrated extract was weighed, and the extraction yield was calculated as: eight of extract / weight of dried powde. y 100%. 2/ 8 Pharmacy Reports bilimbi sunscreen, efficacy and stability Table 1. Composition of sunscreen gel formulations Ingredient Function bilimbi ethanolic extract Carbopol 940 Formula (% w/. Active ingredient Gelling agent Glycerin Humectant Methylparaben Preservative TEA Neutralizing agent Distilled water Solvent up to 100 up to 100 up to 100 up to 100 Phytochemical screening Preliminary phytochemical screening was conducted to identify the presence of major secondary metabolites in the ethanolic extract using standard qualitative methods . Phenolic compounds. Two milliliters of extract was mixed with 10 drops of 1% FeClCE solution. Formation of a green, purple, blue, or dark black precipitate indicated the presence of phenolic compounds . rod, and triethanolamine was added dropwise while stirring continuously until a clear gel base was formed. The A. bilimbi extract was dispersed in glycerin, mixed until homogeneous, and incorporated into the gel The methylparaben solution was then added and mixed thoroughly until a uniform gel was obtained. The final product was transferred into appropriate Flavonoids. Two milliliters of extract was mixed with 100 mL of boiling water . qua fervid. , boiled for 5 minutes, and filtered. Five milliliters of the filtrate was collected, followed by addition of magnesium powder and 1 mL of concentrated HCl, then shaken Development of red, yellow, or orange coloration indicated the presence of flavonoids . Physicochemical characterization Tannins. One to two milliliters of ethanolic extract was treated with 2 to 3 drops of 10% FeClCE solution. color change to greenish or black indicated the presence of tannins . Homogeneity test. A small amount of gel was spread between two glass slides and observed under transmitted light for the presence of undissolved Acceptable gels should exhibit uniform consistency without visible particulate matter . Gel formulation and preparation pH measurement. A pH meter was calibrated using acetate buffer . H 4. and phosphate buffer . H 7. One gram of gel was diluted in 10 mL of distilled water, and the pH was measured. The acceptable pH range for topical gels is 4. 5 to 7. 0, corresponding to the physiological pH of human skin . Four gel formulations were prepared with varying concentrations of A. bilimbi leaf extract: F0 . %, contro. F1 . 2%). F2 . %), and F3 . %). The composition of each formulation is presented in Table The gel base consisted of Carbopol 940 as the gelling agent, glycerin as a humectant, methylparaben as a preservative, triethanolamine as a neutralizing agent, and distilled water as the solvent. The gel was prepared according to the following procedure adapted from Buang et al. : Carbopol 940 was dispersed in hot distilled water at a ratio of 1:20 . and allowed to swell . In a separate beaker, methylparaben was dissolved in hot distilled The swollen Carbopol was stirred with a glass Pharmacy Reports 5. :110 | https://doi. org/10. 51511/pr. Organoleptic evaluation. The color, odor, and texture of each gel formulation were examined visually and recorded. An acceptable gel should exhibit color and aroma consistent with the active ingredient and possess a texture that is neither too fluid nor too viscous . Viscosity determination. Fifty grams of gel was placed in a container, and spindle No. 11 was immersed into the sample. Viscosity was measured using a rotational viscometer at 40 rpm. The acceptable viscosity range for topical gels is 2,000 to 50,000 cps . Spreadability test. A 0. 5 g sample of gel was placed on a 7 cm diameter glass plate, covered with another glass plate, and subjected to a 50 g load for one The diameter of the spread gel was measured. 3/ 8 Pharmacy Reports bilimbi sunscreen, efficacy and stability An acceptable spreadability diameter ranges from 5 to 7 cm . Statistical analysis Adhesiveness test. A 0. 5 g sample of gel was placed between two glass slides, pressed with a 50 g load, and allowed to stand for three minutes. The time required to separate the two glass slides was recorded. Acceptable adhesiveness should exceed 1 second . All measurements were performed in triplicate, and data are expressed as mean A standard deviation. Statistical comparisons between formulations and between pre- and post-stability testing were performed using appropriate statistical tests. Differences were considered statistically significant at p < 0. Accelerated stability testing Results Stability assessment was conducted using a cycling test method over 12 days. Gel samples were stored at 4AC for 24 hours, followed by 40AC for 24 hours, constituting one cycle of 2 days. This procedure was repeated for six complete cycles. Physicochemical parameters . H, viscosity, spreadability, and adhesivenes. were evaluated before and after the stability test . Yield of simplicia and extract The dried leaf powder . of A. bilimbi yielded 22% from the fresh leaves, while the concentrated ethanolic extract yielded 14. 57% from the dried powder. Both yields were in accordance with the standards specified in the Indonesian Herbal Pharmacopoeia. Phytochemical screening SPF value determination Test solutions with a concentration of 20,000 g/mL were prepared from the extract and each gel formulation. Samples were transferred into a 5 mL volumetric flask and diluted to volume with 70% ethanol . SPF values were determined using UV-Vis spectrophotometry according to the Mansur method. Absorbance was recorded at 5 nm intervals from 290 to 320 nm in triplicate. The mean absorbance at each wavelength was multiplied by the corresponding erythema effect (EE) y solar intensity (I) values, and the sum was multiplied by a correction factor (CF) of 10 to obtain the SPF value (Table . The SPF was calculated using the following equation: Qualitative phytochemical analysis of the A. ethanolic extract revealed the presence of phenolic compounds, flavonoids, and tannins (Table . Phenolic compounds were confirmed by the formation of a green precipitate upon addition of 1% FeClCE. Flavonoid presence was indicated by the development of yellow coloration after treatment with magnesium powder and concentrated HCl. Tannins were detected through the appearance of a greenish to black color following addition of 10% FeClCE. Organoleptic characteristics where EE represents the erythemal effect spectrum. I represents the solar intensity spectrum. Abs represents the absorbance of the sunscreen product, and CF is the correction factor with a value of 10. Visual examination revealed that all gel formulations (F0 to F. exhibited acceptable color, odor, and texture both before and after stability testing (Figure . The color intensity increased progressively with higher extract concentrations, ranging from transparent in F0 to dark brown in F3. All formulations displayed a characteristic herbal odor and semi-solid gel texture suitable for topical application. Table 2. Normalized product function used for SPF calculation Homogeneity test Microscopic examination of all gel formulations showed homogeneous dispersion without visible undissolved particles or phase separation, both before and after stability testing (Figure . This indicates uniform distribution of the extract throughout the gel matrix in all formulations. Wavelength (, n. EE y I pH measurement Total The pH values of all formulations ranged from 4. 0, falling within the acceptable range for topical Pharmacy Reports 5. :110 | https://doi. org/10. 51511/pr. 4/ 8 Pharmacy Reports bilimbi sunscreen, efficacy and stability Table 3. Phytochemical screening results of A. bilimbi ethanolic leaf extract Secondary metabolite Reagent Observation Result Phenolic compounds 1% FeClCE Green precipitate formed Positive ( ) Flavonoids Mg powder HCl Yellow color formed Positive ( ) Tannins 10% FeClCE Greenish to black color formed Positive ( ) Image Figure 1. Organoleptic appearance of sunscreen gel formulations containing different concentrations of A. ethanolic extract. Before stability testing, showing F0 . %). F1 . 2%). F2 . %), and F3 . %) from left to right. After stability testing, demonstrating maintained appearance and consistency across all formulations. Figure 2. Homogeneity assessment of sunscreen gel formulations. Before stability testing and . after stability testing, showing uniform dispersion without particulate matter or phase separation across all formulations (F0 to F. Images were captured by spreading gel samples between glass slides under transmitted light. application (Figure 3A). An inverse relationship was observed between extract concentration and pH, with higher concentrations resulting in lower pH values. This pH reduction is attributable to the acidic nature of the A. bilimbi ethanolic extract . H 5. Statistical analysis revealed no significant difference in pH values before and after stability testing . > 0. , indicating pH stability across all Pharmacy Reports 5. :110 | https://doi. org/10. 51511/pr. Viscosity determination Viscosity measurements demonstrated that all formulations met the acceptable range of 2,000 to 50,000 cps (Figure 3B). A decrease in viscosity was observed with increasing extract concentration, both before and after stability testing. Statistical analysis showed no significant difference in viscosity between pre-stability and post-stability samples . > 0. confirming viscosity stability of the formulations. 5/ 8 Pharmacy Reports bilimbi sunscreen, efficacy and stability Figure 3. Physicochemical properties of sunscreen gel formulations before and after stability testing. (A) pH values decreased slightly with extract concentration, remaining within acceptable range . 5Ae7. (B) Viscosity maintained acceptable values . ,000Ae50,000 cp. across formulations. (C) Spreadability increased with extract concentration. (D) Adhesiveness decreased with extract concentration but remained above minimum requirement (>1 secon. Data: mean A SD . F0 = F1 = 0. F2 = 1%. F3 = 5% extract. Green line: before testing. orange line: after testing. Spreadability test The spreadability of gel formulations increased proportionally with extract concentration (Figure 3C). All formulations exhibited spreadability diameters within the acceptable range of 5 to 7 cm. The enhanced spreadability at higher extract concentrations is associated with the reduced viscosity of these formulations. Adhesiveness test Adhesiveness measurements revealed a decreasing trend with increasing extract concentration (Figure 3D). Statistical analysis indicated a significant difference between pre-stability and post-stability values . < 0. suggesting reduced stability of adhesive properties. However, all formulations maintained adhesiveness values exceeding the minimum requirement of 1 second, thereby meeting the acceptable standard for topical gels. SPF value determination Spectrophotometric analysis demonstrated that SPF values increased proportionally with extract concentration (Figure . This correlation is attributed to the higher content of photoprotective secondary metabolites, particularly flavonoids and phenolic Pharmacy Reports 5. :110 | https://doi. org/10. 51511/pr. compounds, at elevated extract concentrations . Among all formulations. F3 containing 5% A. leaf extract exhibited the highest SPF value of 36. categorized as ultraprotection. F2 . % extrac. also achieved ultraprotection category, while F1 . demonstrated maximum protection category. Following accelerated stability testing, a reduction in SPF values was observed across all formulations (Figure . This decrease is likely attributed to thermal degradation of the photoprotective compounds in the A. bilimbi extract during exposure to cycling temperatures . AC and 40AC). Despite this reduction, statistical analysis indicated no significant difference between pre-stability and post-stability SPF values . > 0. , suggesting acceptable stability of the photoprotective efficacy. Discussion This study successfully developed and characterized sunscreen gel formulations containing A. ethanolic leaf extract at varying concentrations . %, 2%, 1%, and 5%). The findings demonstrate that all formulations exhibited acceptable physicochemical properties, including organoleptic characteristics, homogeneity, pH, viscosity, spreadability, and adhesiveness, meeting the established standards for 6/ 8 Pharmacy Reports bilimbi sunscreen, efficacy and stability Figure 4. SPF values of sunscreen gel formulations before and after stability testing. SPF increased with extract concentration, with F3 . % extrac. showing highest photoprotection (SPF 36. A slight, non-significant decrease in SPF occurred after stability testing . > 0. Data: mean A SD . F0 = 0%. F1 = 0. F2 = 1%. F3 = 5% extract. Dotted lines: SPF thresholds for maximum protection . Ae. and ultraprotection (>. Green line: before testing. orange line: after testing. topical gel preparations. Stability assessment revealed that pH, viscosity, spreadability, and SPF values remained stable under accelerated conditions, while adhesiveness showed reduced stability but maintained acceptable performance. The photoprotective efficacy, measured as SPF values, increased proportionally with extract concentration, with F1 achieving maximum protection and F2 and F3 reaching ultraprotection These results establish a clear concentrationdependent relationship between A. bilimbi extract content and sunscreen effectiveness. irritation and maintaining the skin barrier function during topical application. The stability of pH values throughout the accelerated aging test . > 0. further confirms the formulationAos resistance to pH drift under environmental stress. The organoleptic evaluation revealed progressive color intensification from transparent to dark brown with increasing extract concentration. This chromatic change is attributable to the tannin content in A. Tannins are polyphenolic compounds that exhibit high solubility in polar solvents and characteristically impart brown coloration to solutions and formulations . The maintained organoleptic consistency before and after stability testing indicates that the formulations are resistant to visual degradation under thermal stress, which is essential for product shelf life and consumer The observed decrease in viscosity with increasing extract concentration presents an interesting rheological This reduction is likely caused by the pHdependent swelling behavior of Carbopol 940, the gelling agent employed in this study. Carbopol polymers achieve optimal gelation and maximum viscosity at neutral to slightly alkaline pH through ionization of carboxyl groups and subsequent polymer chain expansion . As the extract lowers the formulation pH, the degree of Carbopol ionization decreases, resulting in reduced polymer swelling and lower viscosity. Additionally, exposure to extreme temperatures during stability testing may compromise the three-dimensional network structure of Carbopol 940, further contributing to viscosity reduction . Nevertheless, the viscosity of all formulations remained within the acceptable range of 2,000 to 50,000 cps, ensuring appropriate consistency for topical application. The inverse relationship between extract concentration and pH values observed in this study can be explained by the acidic nature of the A. bilimbi ethanolic extract . H 5. As the proportion of extract increases in the formulation, the overall pH decreases accordingly. Despite this pH reduction, all formulations remained within the physiologically acceptable range of 4. 5 to 0, which corresponds to the pH of human skin . This pH compatibility is crucial for minimizing skin The spreadability and adhesiveness properties exhibited inverse trends relative to viscosity changes. Higher extract concentrations, which correspond to lower viscosity, demonstrated enhanced spreadability. This relationship is consistent with fundamental rheological principles, as reduced internal resistance facilitates easier deformation and spreading of the gel matrix . Conversely, adhesiveness decreased with increasing extract concentration and showed significant Pharmacy Reports 5. :110 | https://doi. org/10. 51511/pr. 7/ 8 Pharmacy Reports variation after stability testing . < 0. The reduced adhesiveness is attributed to the diminished ability of the gelling agent to maintain intermolecular cohesion at lower pH and after thermal stress . However, it is important to note that despite the statistical variation, all formulations maintained adhesiveness exceeding 1 second, thereby satisfying the minimum requirement for topical gel preparations. The accelerated stability testing using cycling test methodology provided valuable insights into the formulation behavior under thermal stress. The cycling between low . AC) and high . AC) temperatures simulates extreme storage conditions and accelerates potential degradation processes. While most physicochemical parameters demonstrated acceptable stability, the adhesiveness reduction suggests some structural changes in the gel network. This finding highlights the importance of optimizing storage conditions to maintain optimal product performance throughout the shelf life. The observed decrease in SPF values following stability testing, although not statistically significant . > 0. , warrants careful consideration. Prolonged exposure to elevated temperatures may induce degradation of photoprotective compounds, particularly flavonoids and phenolic derivatives present in the A. bilimbi extract. Previous research has demonstrated that A. bilimbi ethanolic extracts are thermally sensitive and undergo degradation at temperatures exceeding 40AC . The cycling test protocol employed in this study subjected the formulations to 40AC for extended periods, potentially compromising the stability of heatlabile bioactive compounds. This thermal sensitivity underscores the necessity for appropriate storage conditions and suggests that cold storage or the incorporation of stabilizing agents may be beneficial for maintaining photoprotective efficacy. The concentration-dependent increase in SPF values represents the most significant finding of this The SPF values ranged from negligible protection in the control formulation (F. to maximum protection in F1 . 2% extrac. and ultraprotection in F2 . % extrac. and F3 . % extract. SPF 36. This dose-response relationship directly correlates with the concentration of photoprotective secondary metabolites in the formulations. The phytochemical screening confirmed the presence of flavonoids, phenolic compounds, and tannins, all of which possess UV-absorbing properties through their conjugated aromatic systems and chromophoric groups . Pharmacy Reports 5. :110 | https://doi. org/10. 51511/pr. bilimbi sunscreen, efficacy and stability Flavonoids are particularly effective UV absorbers due to their aromatic ring structures with hydroxyl substituents, which enable efficient absorption of UV radiation in the 290 to 320 nm range. Phenolic compounds similarly contribute to photoprotection through their ability to absorb UV energy and dissipate it through non-radiative decay processes. The presence of these compounds in higher concentrations within F2 and F3 explains their superior photoprotective Additionally, these phytochemicals may exert antioxidant effects by scavenging reactive oxygen species generated during UV exposure, providing a dual mechanism of skin protection. The findings of this study suggest that formulation F3, containing 5% A. bilimbi ethanolic extract, offers the highest photoprotective efficacy with an SPF value 9, categorizing it as ultraprotection. However, practical formulation decisions must balance efficacy with other considerations such as aesthetic properties, stability, and cost-effectiveness. The lower viscosity and adhesiveness observed in F3 may affect consumer perception and product performance during application. Furthermore, the darker brown coloration resulting from higher tannin content might be cosmetically less acceptable to certain consumer segments. Formulation F2, containing 1% extract, presents a potentially optimal compromise, achieving ultraprotection (SPF >. while maintaining more favorable physicochemical properties compared to F3. The selection between F2 and F3 would depend on the intended product positioning and target consumer preferences. For applications requiring maximum photoprotection, such as beach or sports formulations. F3 would be preferable. For daily-use cosmetic products where aesthetic properties are prioritized. F2 may offer better overall performance. The development of natural sunscreen agents has gained considerable attention due to growing consumer preference for plant-based cosmetic products and concerns regarding the safety and environmental impact of synthetic UV filters. The present study contributes to this field by demonstrating that A. bilimbi leaf extract can serve as an effective natural photoprotective agent. While previous research has explored various topical applications of A. bilimbi extracts, including bath soaps, antioxidant creams, and peel-off masks . , this investigation represents the first systematic evaluation of gel formulations specifically designed for sunscreen 8/ 8 Pharmacy Reports The photoprotective efficacy demonstrated in this study positions A. bilimbi extract as a competitive natural alternative to synthetic UV filters. However, it is important to acknowledge that natural photoprotective agents typically require higher concentrations to achieve SPF values comparable to synthetic compounds. This concentration dependency must be balanced against potential skin sensitization, color interference, and formulation stability challenges that may arise at elevated extract levels. While these results are promising, several areas require further investigation. Formulation strategies such as microencapsulation or antioxidant stabilizers should be explored to enhance thermal stability. Comprehensive safety evaluations, including skin irritation and sensitization tests, are needed before clinical use. Long-term stability studies under realworld conditions would better predict shelf life than accelerated testing. Future research should assess broad-spectrum photoprotection, including UV-A defense not evaluated here. Clinical studies with human subjects are needed to confirm in vivo efficacy. Additionally, optimizing the gel base to improve adhesiveness at higher extract concentrations could enhance overall formulation performance. Conclusion This study demonstrates that sunscreen gel formulations containing A. bilimbi ethanolic leaf extract exhibit acceptable physicochemical properties and concentration-dependent photoprotective efficacy. Formulations with 1% and 5% extract achieved ultraprotection (SPF >. , establishing A. bilimbi as a promising natural sunscreen ingredient. Stability testing revealed generally stable physicochemical parameters, though thermal sensitivity of photoprotective compounds indicates the need for optimized storage These findings provide a foundation for developing natural, plant-based sunscreen products and highlight the potential of A. bilimbi leaf extract in cosmetic photoprotection applications. Acknowledgements The authors thank all those who contributed to this study. Pharmacy Reports 5. :110 | https://doi. org/10. 51511/pr. bilimbi sunscreen, efficacy and stability Funding None. Author contributions Conceptualization. RGW. Methodology and investigation. RGW and AMR. Data curation. RGW and UKSR. Formal analysis and writingAioriginal draft. RGW. WritingAireview and editing. RGW. AMR, and UKSR. Supervision. AMR. Declaration of interest The authors declare no competing interests. Received: October 27, 2025 Revised: November 15, 2025 Accepted: November 16, 2025 Published: December 31, 2025 References