Salicylic acid 12.5% / Camphor 3.11% liquid
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Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing all 17 studies.
Reviews & meta-analyses: 3 · 2017–2026
Showing all 17 studies, sorted by most relevant.
M. El-Esawi, H. Elansary, N. El-Shanhorey, et al.
Frontiers in Physiology, 2017
Salinity stress as a major agricultural limiting factor may influence the chemical composition and bioactivity of Rosmarinus officinallis L. essential oils and leaf extracts. The application of salicylic acid (SA) hormone may alleviate salinity stress by modifying the chemical composition, gene expression and bioactivity of plant secondary metabolites. In this study, SA was applied to enhance salinity tolerance in R. officinallis. R. officinallis plants were subjected to saline water every two days (640, 2000 and 4000 ppm NaCl) and 4 biweekly sprays of SA at 0,100, 200 and 300 ppm for 8 weeks. Simulated salinity reduced all vegetative growth parameters such as plant height, plant branches and fresh and dry weights. However, SA treatments significantly enhanced these plant growth and morphological traits under salinity stress. Salinity affected specific major essential oils components causing reductions in α-pinene, β-pinene and cineole along with sharp increases in linalool, camphor, borneol and verbenone. SA applications at 100-300 ppm largely reversed the effects of salinity. Interestingly, SA treatments mitigated salinity stress effects by increasing the total phenolic, chlorophyll, carbohydrates and proline contents of leaves along with decline in sodium and chloride. Importantly, this study also proved that SA may stimulate the antioxidant enzymatic mechanism pathway including catalase (CAT), superoxide dismutase (SOD) and ascorbate peroxidase (APX) as well as increasing the non-enzymatic antioxidants such as free and total ascorbate in plants subjected to salinity. Quantitative real-time PCR analysis revealed that APX and 3 SOD genes showed higher levels in SA-treated rosemary under salinity stress, when compared to non-sprayed plants. Moreover, the expression level of selected genes conferring tolerance to salinity (bZIP62, DREB2, ERF3 and OLPb) were enhanced in SA-treated rosemary under salt stress, indicating that SA treatment resulted in the modulation of such genes expression which in turn enhanced rosemary tolerance to salinity stress.
Abstract licence: CC BY
Razzaq A, Zafar MM, Ali A, et al.
2025
Plant metabolites play a vital role in a plant’s defense system. Plant metabolites are extensively studied for their therapeutic values. Plant therapeutic values are attributed based on the magnitude of metabolites. Among all the metabolites, secondary metabolites are considered to have more potential. Different medicinal plants like Cephalotaxus contain therapeutically valuable bioactive alkaloids. The pharmaceutical relevance of secondary metabolites has been well recognized, but low accumulation and convoluted biosynthetic mechanism hamper their industrial production. Elicitors, both biotic and abiotic, have emerged as effective strategies to enhance metabolite biosynthesis by triggering plant defense signaling pathways. Chemical agents like salicylic acid, methyl jasmonate, nitric oxide, and heavy metals, along with physical factors such as ultraviolet radiation, salinity, and osmotic stress, significantly increase secondary metabolite production. Similarly, microbial extracts, polysaccharides, and polyamines serve as potent biotic elicitors. Synergistic combinations, particularly sodium fluoride with methyl jasmonate, have shown remarkable success in boosting Cephalotaxus alkaloid yields. Advances in elicitor-mediated interventions, coupled with omics, nanotechnology, and CRISPR-based bioprocessing, promise sustainable and scalable production systems. This review highlights the mechanisms, case studies, challenges, and prospects of elicitor applications, emphasizing their transformative role in bridging traditional medicinal plants with modern pharmaceutical needs.
Abstract licence: CC BY
O. Filimonova, Y. Shishkova, A. Vereshchagin
Actual problems in dentistry, 2025
The purpose of the review is to emphasize the importance of integrating hydrolates into modern dental practice as a safe and effective approach to the treatment and prevention of dental diseases. The article discusses the use of hydrolates in dental practice for the symptomatic treatment of oral diseases. Hydrolate is a secondary distillate, fragrant (florentine) water formed during steam distillation of vegetable (usually essential oil) raw materials. Any hydrolate consists of distilled water and components that are carried away from vegetable raw materials by steam during steam or water distillation. Hydrolates have unique properties that can be useful in various aspects of dentistry. Hydrolates are one of the new directions in the complex treatment of inflammatory diseases of the oral cavity. Hydrolates are rich in useful bioactive substances, vitamins and minerals, they contain various components: flavonoids, tannins, salicylic acid, camphor, quercetin, runines and terpenes. The modern literature on dental care is paying more and more attention to natural therapeutic products along with commercially created alternatives. Hydrolatotherapy, unlike prescription pharmaceuticals, can treat several symptoms at once or be used in combination with traditional treatments. The analysis of the available literature allows us to conclude about the positive prospects for the use of hydrolates in dental practice as anti-inflammatory, antimicrobial, regenerating, and bleeding-reducing drugs. Further controlled clinical studies are needed to establish the proven effectiveness of hydrolates and their widespread use as medicinal ingredients, determine the appropriate dose, bioavailability and bioefficiency.
Abstract licence: CC BY
Shabbir A, Parvinzadeh Gashti M
2026
G. Nițulescu, D. Lupuliasa, Ines Adam-Dima, et al.
Cosmetics, 2023
Sunscreens reduce the occurrence risk of skin disorders such as sunburn, skin aging, and cancer through their ability to absorb, reflect, and scatter ultraviolet (UV) radiation. This review provides an overview of UV filters as active ingredients of sunscreen products, emphasizing their classification and structural characteristics. Their photostability, mechanism of action of ultraviolet radiation absorption, optical properties, and regulatory status are discussed based on their chemical structure. The main classes of organic UV filters presented include aminobenzoic acid derivatives, salicylic acid derivatives, cinnamic acid derivatives, benzophenones, dibenzoylmethane derivatives, benzylidene camphor derivatives, triazines, benzimidazole derivatives, and benzotriazole derivatives. The pursuit of new UV filters through research is crucial in advancing sunscreen technology and ensuring the availability of effective and safe options for sun protection.
Abstract licence: CC BY
P. Bednarczyk, Anna Nowak, Wiktoria Duchnik, et al.
International Journal of Molecular Sciences, 2023
- Allantoin
- Ibuprofen
- Adhesives
This study investigated the impact of various enhancers on permeation through the skin and accumulation in the skin from acrylic pressure-sensitive adhesive-based drug-in-adhesives matrix-type transdermal patches. Eleven patches, each containing a 5% enhancer of permeation, encompassing compounds such as salicylic acid, menthol, urea, glycolic acid, allantoin, oleic acid, Tween 80, linolenic acid, camphor, N-dodecylcaprolactam, and glycerin, were developed. Ibuprofen (IBU) was the model active substance, a widely-used non-steroidal anti-inflammatory drug. The results were compared to patches without enhancers and commercial preparations. The study aimed to assess the effect of enhancers on IBU permeability. The adhesive properties of the patches were characterised, and active substance permeability was tested. The findings revealed that patches with 5% allantoin exhibited the highest IBU permeability, approximately 2.8 times greater than patches without enhancers after 24 h. These patches present a potential alternative to commercial preparations, highlighting the significant impact of enhancers on transdermal drug delivery efficiency.
Abstract licence: CC BY
El-Hefny M, Hussien MK
2025
- Humic Substances
- Oils, Volatile
- Plant Extracts
Natural extracts as biostimulants have the potential to enhance the productivity and growth of many medicinal and aromatic plants. This study aimed to enhance the growth, and essential oil (EO) content, as well as composition of Lavandula latifolia Medik. by using Malva parviflora L. extract (ME) as a biostimulant in combination with humic acid (HA) in a field experiment in two successive seasons of 2022 and 2023. The phenolic, flavonoid and water-soluble vitamins of the ME were analyzed using an HPLC. The protein amino acids of the ME were identified by an amino acid analyzer. The prepared concentrations of HA (0, 1, 2, and 4 g/L) were applied to the soil. While, they for ME (0, 2, 4, and 6 g/L) were added as a foliar spray. The EO compositions collected from the leaves of the treated L. latifolia plants were subjected to the hydro-distillation method and analyzed using GC-MS. The most prevalent vitamins found in ME were vitamin B12, vitamin C, and folic acid. Besides, several phenolic compounds were found in ME, such as catechol, cinnamic acid and syringic acid, while flavonoid chemicals, such as luteolin and quercetin. Also, alanine, ammonia, aspartic acid, glutamic acid, glycine, and tyrosine were the ME's most prominent nitrogenous and amino acid components. The most effective treatments of HA and ME on the plant height, the number of branches/plant, and plant fresh weight were 4 + 6 g/L and 4 + 2 g/L for leaf area and chlorophyll content, it was 4 + 4 g/L; and for EO percentage were 4 + 0 g/L, 2 + 0 g/L, and 4 + 4 g/L, compared to the control treatment for each characteristic. The main EO compounds eucalyptol, camphor, α-pinene, β-pinene, Δ-elemene, germacrene D-4-ol, isoborneol, β-caryophyllene oxide, and tau.-cadinol identified in the leaves were found in the range of 28.74-46.19%, 15.34-30.49%, 3.39-7.16%, 0-5.08%, 0-5.18%, 0-3.20%, 0-3.31% and 0-3.40%, respectively. It can be concluded that a combination treatment of HA and ME as natural biostimulant compounds at 4 + 4 g/L could be recommended for good plant growth, and EO quantity of L. latifolia plants.
Abstract licence: CC BY
Mueangnak K, Kitwetcharoen H, Thanonkeo S, et al.
2025
- Antioxidants
- Acetates
- Cells, Cultured
Abstract Celosia argentea is a plant known for producing bioactive compounds, including betalains, which possess various biological and pharmaceutical properties. This study aimed to investigate the effect of biotic and abiotic elicitors on betalains production and their antioxidant activity in cell suspension cultures of C. argentea . Various concentrations of chitosan, yeast extract, salicylic acid, methyl jasmonate, copper sulfate (CuSO 4 ), and cobalt chloride (CoCl 2 ) were evaluated. The results revealed that chitosan, salicylic acid, methyl jasmonate, and CuSO 4 significantly improved betalains production in the cell suspension cultures. Among these elicitors, chitosan at 5.0 mg/L and CuSO 4 at 6.4 µM were the most effective in enhancing betalains production, yielding the highest concentrations of 4.65 and 4.99 mg/g dry weight, respectively. Notably, the betalains derived from the elicitor-treated cultures exhibited greater antioxidant activity compared to the control. These findings suggest that chitosan and CuSO 4 are promising elicitors for sustainable in vitro production of betalains from C. argentea cell suspension cultures on a commercial scale, owing to their ability to enhance betalains production and antioxidant activity.
Abstract licence: CC BY
B. Dinçel, E. Beyzi
Journal of Plant Nutrition, 2024
Liu B, Qin Q, Hu J, et al.
2025
Rice sheath rot has progressively developed into a growing threat to global rice production, particularly in intensively managed systems conducive to disease development. Therefore, accurate identification of the causal pathogen and the development of sustainable management strategies represent urgent scientific requirements. In this study, we isolated the causal organism of rice sheath rot from infected rice tissues and identified it as Fusarium verticillioides based on multi-locus sequence analysis. Eight endophytic bacterial strains were recovered from healthy rice root systems. Among the isolates, Bacillus velezensis isolate 7-A exhibited the strongest antifungal activity against F. verticillioides. This isolate demonstrated broad-spectrum antifungal activity, with inhibition rates ranging from 54.8% to 71.8%. Phylogenetic analysis based on 16S rRNA and gyrB gene sequences identified it as B. velezensis. Further characterization revealed that B. velezensis 7-A is capable of secreting proteases and synthesizing siderophores. The filtered liquid from sterile fermentation markedly inhibited the growth of mycelium in F. verticillioides and induced marked morphological abnormalities. Liquid LC-MS analysis identified multiple antifungal active substances, including camphor, ginkgolides B, salicin, cinnamic acid, hydroxygenkwanin, stearamide, β-carotene, and others. A pot experiment demonstrated that the fermentation broth of B. velezensis 7-A effectively suppressed the occurrence of rice sheath rot, achieving a relative control efficacy of 61.3%, which is comparable to that of a 10% carbendazim water-dispersible granule (WDG). Additionally, isolate 7-A enhances plant disease resistance by activating the activities of key defense enzymes. These findings provide preliminary insights into its potential application in integrated and sustainable disease management programs.
Abstract licence: CC BY
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.