A Long-Lasting Triamcinolone-Loaded Microneedle Patch for Prolonged Dermal Delivery

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY Iranian Journal of Pharmaceutical Research Pub Date : 2024-02-27 DOI:10.5812/ijpr-138857
Nasrin Zarei Chamgordani, S. Asiaei, F. Ghorbani‐Bidkorpeh, Masoud Babaee Foroutan, Mostafa Dahmardehei, Hamid Reza Moghimi
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Abstract

Background: Scar is an unpleasant skin lesion that occurs following deep wounds or burns. The application of local triamcinolone is a common treatment for scar treatment and prevention, which should be repeated several times in conventional dosage forms. An effort has been made here to provide a prolonged triamcinolone dermal delivery by microneedle technology, which can also be used for wound closure. Objectives: This study aimed to develop a long-lasting polylactic acid (PLA) microneedle patch for the prolonged release of triamcinolone acetonide (TrA) that could potentially be used for closure of wound edges and scar prevention and treatment. Methods: In this study, 3% and 10% TrA-containing polymeric microneedles were fabricated using the micro molding-solvent casting method. Optical microscopy, X-ray diffraction analysis (XRD), Fourier-transform infrared spectroscopy (FT-IR), and differential scanning calorimetry (DSC) were used for the characterization of microneedles. Mechanical strength was evaluated using a compression test and methylene blue staining. Additionally, the insertion depth was determined by histopathological sectioning of human skin samples and also insertion into Parafilm®M as a skin model. The in vitro drug release profile of the microneedles was studied over 34 days, and the kinetic model was determined. The ex-vivo skin permeation of TrA was studied using a Franz-diffusion cell. Results: The TrA-containing PLA microneedles were fabricated with a uniform structure without any failure, deterioration, or loss of needles. Fourier-transform infrared spectroscopy and differential scanning calorimetry showed no interaction between TrA and PLA, and no effect on crystallinity and thermal behavior of TrA on polymer was detected. Microneedles showed appropriate mechanical properties, which were able to penetrate to about 900 - 1000 μm depth. Release profile from the whole body of 10% and 3% microneedle fitted to Higuchi model with cumulative amounts of 625 µg and 201.64 µg over 34 days. Release from the needles followed zero-order kinetic with cumulative amounts of 30.04 µg and 20.36 µg for 10% and 3%, respectively, for 34 days. Permeation was calculated to be 17 µg/day for 10% TrA-containing microneedle. Conclusions: The results suggested that suitable PLA microneedles containing TrA with prolonged release behavior can be successfully constructed with the solvent casting method.
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用于延长皮肤给药时间的长效曲安奈德微针贴片
背景:疤痕是一种令人不快的皮肤损伤,发生在深度创伤或烧伤之后。局部使用曲安奈德是治疗和预防疤痕的常用方法,但传统剂型需重复使用多次。本文试图通过微针技术提供一种可用于伤口闭合的长效三苯氧胺皮肤给药方法。研究目的本研究旨在开发一种长效聚乳酸(PLA)微针贴片,用于延长曲安奈德(TrA)的释放时间,可用于伤口边缘的闭合以及疤痕的预防和治疗。研究方法本研究采用微成型-溶剂浇注法制造了含 3% 和 10% TrA 的聚合物微针。使用光学显微镜、X 射线衍射分析(XRD)、傅立叶变换红外光谱(FT-IR)和差示扫描量热法(DSC)对微针进行表征。使用压缩试验和亚甲基蓝染色评估了机械强度。此外,还通过对人体皮肤样本进行组织病理学切片,以及插入作为皮肤模型的 Parafilm®M 来确定插入深度。研究了微针 34 天的体外药物释放曲线,并确定了动力学模型。使用弗朗兹扩散池研究了 TrA 的体外皮肤渗透情况。结果显示制成的含 TrA 聚乳酸微针结构均匀,没有出现任何失效、变质或掉针现象。傅立叶变换红外光谱法和差示扫描量热法显示,TrA 和聚乳酸之间没有相互作用,也没有检测到 TrA 对聚合物结晶度和热行为的影响。微针显示出适当的机械性能,能够穿透约 900 - 1000 μm 的深度。10% 和 3% 微针的全身释放曲线符合樋口模型,34 天内的累积量分别为 625 微克和 201.64 微克。针头的释放遵循零阶动力学,10%和 3%的微针在 34 天内的累积量分别为 30.04 微克和 20.36 微克。根据计算,含 10% TrA 的微针的渗透量为 17 微克/天。结论研究结果表明,采用溶剂浇铸法可以成功地制造出合适的含TrA的微针,并能延长释放时间。
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来源期刊
CiteScore
3.40
自引率
6.20%
发文量
52
审稿时长
2 months
期刊介绍: The Iranian Journal of Pharmaceutical Research (IJPR) is a peer-reviewed multi-disciplinary pharmaceutical publication, scheduled to appear quarterly and serve as a means for scientific information exchange in the international pharmaceutical forum. Specific scientific topics of interest to the journal include, but are not limited to: pharmaceutics, industrial pharmacy, pharmacognosy, toxicology, medicinal chemistry, novel analytical methods for drug characterization, computational and modeling approaches to drug design, bio-medical experience, clinical investigation, rational drug prescribing, pharmacoeconomics, biotechnology, nanotechnology, biopharmaceutics and physical pharmacy.
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