首页> 外文期刊>Journal of Turbulence >Fabrication, Physicochemical Characterization, and Performance Evaluation of Biodegradable Polymeric Microneedle Patch System for Enhanced Transcutaneous Flux of High Molecular Weight Therapeutics
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Fabrication, Physicochemical Characterization, and Performance Evaluation of Biodegradable Polymeric Microneedle Patch System for Enhanced Transcutaneous Flux of High Molecular Weight Therapeutics

机译:生物降解聚合物微针贴剂系统的制备,物理化学表征和性能评价,用于增强高分子量治疗的经皮通量

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A revolutionary paradigm shift is being observed currently, towards the use of therapeutic biologics for disease management. The present research was focused on designing an efficient dosage form for transdermal delivery of alpha-choriogonadotropin (high molecular weight biologic), through biodegradable polymeric microneedles. Polyvinylpyrrolidone-based biodegradable microneedle arrays loaded with high molecular weight polypeptide, alpha-choriogonadotropin, were fabricated for its systemic delivery via transdermal route. Varied process and formulation parameters were optimized for fabricating microneedle array, which in turn was expected to temporally rupture the stratum corneum layer of the skin, acting as a major barrier to drug delivery through transdermal route. The developed polymeric microneedles were optimized on the basis of quality attributes like mechanical strength, axial strength, insertion ratio, and insertion force analysis. The optimized polymeric microneedle arrays were characterized for in vitro drug release studies, ex vivo drug permeation studies, skin resealing studies, and in vivo pharmacokinetic studies. Results depicted that fabricated polymeric microneedle arrays with mechanical strength of above 5 N and good insertion ratio exhibited similar systemic bioavailability of alpha-choriogonadotropin in comparison to marketed subcutaneous injection formulation of alpha-choriogonadotropin. Thus, it was ultimately concluded that the designed drug delivery system can serve as an efficient tool for systemic delivery of therapeutic biologics, with an added benefit of overcoming the limitations of parenteral delivery, achieving better patient acceptability and compliance.
机译:目前正在观察到一种革命性的范式转变,即使用治疗性生物制剂进行疾病管理。本研究的重点是设计一种有效的剂型,通过可生物降解的聚合物微针经皮给药α-绒毛膜促性腺激素(高分子量生物制剂)。制备了以聚乙烯吡咯烷酮为基础的可生物降解微针阵列,该阵列负载有高分子量多肽α-绒毛膜促性腺激素,通过经皮途径进行全身给药。为制备微针阵列,对各种工艺和配方参数进行了优化,从而使皮肤角质层暂时破裂,成为药物经皮给药的主要屏障。根据机械强度、轴向强度、插入比和插入力分析等质量属性,对开发的聚合物微针进行了优化。优化的聚合物微针阵列用于体外药物释放研究、体外药物渗透研究、皮肤再密封研究和体内药代动力学研究。结果显示,机械强度大于5N且插入率良好的聚合物微针阵列与上市的α-绒毛膜促性腺激素皮下注射制剂相比,表现出类似的α-绒毛膜促性腺激素系统生物利用度。因此,最终得出结论,所设计的药物递送系统可以作为治疗性生物制剂系统递送的有效工具,具有克服肠外递送限制的额外益处,实现更好的患者可接受性和依从性。

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