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用于肌肉骨骼疼痛管理的Yataprasen成膜喷雾剂的研发、优化及稳定性研究。

Development, Optimization, and Stability Study of a Yataprasen Film-Forming Spray for Musculoskeletal Pain Management.

作者信息

Angsusing Jaenjira, Samee Weerasak, Tadtong Sarin, Mangmool Supachoke, Okonogi Siriporn, Toolmal Nopparut, Chittasupho Chuda

机构信息

Ph.D. Degree Program in Pharmacy, Faculty of Pharmacy, Chiang Mai University, CMU Presidential Scholarship, Chiang Mai 50200, Thailand.

Department of Thai Traditional and Alternative Medicine, Ministry of Public Health, Bangkok 10100, Thailand.

出版信息

Gels. 2025 Jan 15;11(1):64. doi: 10.3390/gels11010064.

Abstract

Yataprasen (YTPS) remedy ethanolic spray, one of the National Thai Traditional Medicine Formulary, is extensively employed in Thai traditional healthcare to manage musculoskeletal pain and inflammation. Despite its widespread use, the quality and stability of the YTPS formulation, critical to its efficacy, safety, and patient adherence, have not been comprehensively studied. This research developed and optimized a film-forming spray (FFS) formulation of YTPS ethanolic extract and conducted a 6-month stability evaluation. The FFS shares similarities with gel formulations, particularly in its ability to form a cohesive, semi-solid film upon application, enhancing localized drug delivery and prolonged contact time. Key physicochemical properties, including density (0.8450-0.9086 g/cm), pH (4.72-4.95), spray angle (55.58-60.10°), evaporation time (1.04-1.27 min), and theoretical film thickness (7.72-13.97 µm), were analyzed across varying storage conditions. Active components β-amyrin and stigmasterol demonstrated retention rates of 96.78% and 68.22%, respectively, under refrigerated conditions, with degradation rates accelerating at higher temperatures. Significant variations in density, spray angle, film thickness, and stigmasterol concentration were observed. Additionally, the RP-HPLC method was validated for the accurate and precise quantification of the bioactive compounds such as β-amyrin and stigmasterol, demonstrating excellent linearity within a 10-100 µg/mL range for both compounds with excellent linearity R > 0.999. The results confirmed that YTPS-FFS exhibits good stability and that the validated HPLC method is reliable for routine quality control. These findings supported the potential of YTPS-FFS formulation as a standardized and effective dosage form for managing musculoskeletal conditions, advancing its role in modernized traditional medicine.

摘要

泰国国家传统医学配方之一的亚他普瑞森(YTPS)疗法乙醇喷雾,在泰国传统医疗保健中被广泛用于治疗肌肉骨骼疼痛和炎症。尽管其使用广泛,但对于YTPS制剂的质量和稳定性(这对其疗效、安全性和患者依从性至关重要)尚未进行全面研究。本研究开发并优化了YTPS乙醇提取物的成膜喷雾(FFS)制剂,并进行了为期6个月的稳定性评估。FFS与凝胶制剂有相似之处,特别是在应用后能够形成粘性半固体薄膜,增强局部药物递送并延长接触时间。在不同储存条件下分析了关键的物理化学性质,包括密度(0.8450 - 0.9086 g/cm)、pH值(4.72 - 4.95)、喷雾角度(55.58 - 60.10°)、蒸发时间(1.04 - 1.27分钟)和理论薄膜厚度(7.72 - 13.97 µm)。活性成分β-香树脂醇和豆甾醇在冷藏条件下的保留率分别为96.78%和68.22%,在较高温度下降解速率加快。观察到密度、喷雾角度、薄膜厚度和豆甾醇浓度有显著变化。此外,反相高效液相色谱法(RP - HPLC)经验证可准确、精确地定量分析β-香树脂醇和豆甾醇等生物活性化合物,两种化合物在10 - 100 µg/mL范围内均表现出良好的线性,线性相关系数R > 0.999。结果证实YTPS - FFS具有良好的稳定性,且经验证的HPLC方法对于常规质量控制是可靠的。这些发现支持了YTPS - FFS制剂作为治疗肌肉骨骼疾病的标准化有效剂型的潜力,推动了其在现代传统医学中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/668c/11764686/b269cc3324c7/gels-11-00064-g001.jpg

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