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首页> 外文期刊>Materials science & engineering >Design, characterization, and modeling of a chitosan microneedle patch for transdermal delivery of meloxicam as a pain management strategy for use in cattle
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Design, characterization, and modeling of a chitosan microneedle patch for transdermal delivery of meloxicam as a pain management strategy for use in cattle

机译:壳聚糖微针贴片的设计,表征和建模,用于母昔康透皮递送作为牛疼痛管理策略

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This work describes the formulation and evaluation of a chitosan microneedle patch for the transdermal delivery of meloxicam to manage pain in cattle. Microneedle patches composed of chitosan and chitosan/meloxicam were evaluated regarding their chemical composition, uniformity of physical characteristics, capacity to penetrate the skin, and response to thermal and thermo-mechanical changes. Microneedle patches were prepared by varying the percentage of acetic acid used during solution preparation, including 90% (v/v), 50% (v/v), and 10% (v/v). In addition, drug release was assessed by modeling different percentages of penetration into the skin and the number of microneedles on the microneedle patch. Scanning electron microscopy confirmed the presence of microneedles uniformly organized on the patch surface for each percentage of acetic acid used. Fourier transform infrared spectroscopy revealed that 10% (v/v) of acetic acid in the solution was a suitable condition to preserve the characteristic bands of chitosan (amide I and amide II) and meloxicam (amine NeH stretch and C=O stretch) as compared to 90% (v/v) and 50% (v/v) of acetic acid used during the solution preparation. The resultant microneedle patches were successful in penetrating the skin in a cow's cadaver ear. Results demonstrated that the average depth penetration measured after complete dehydration of the penetrated skin was approximately 78 +/- 1 mu m. Chitosan and chitosan/meloxicam microneedle patches with higher acetic acid percentages reflected greater resistance to compressive force as temperature increased. Time-dependent simulation of the transport of diluted species by COMSOL revealed that the transdermal drug delivery increases in function to the increment of the number of microneedles on the surface patch and percentage of penetration per microneedle. One patch released a drug concentration of 3.57 x 10(-5) mol/m(3) in the skin per week, which represents the 26.2% of what is needed for pain management in cattle, established as 1.43 x 10(-4) mol/m(3). These results demonstrate that chitosan/meloxicam microneedles patches may be suitable to manage pain in cattle after routine procedures.
机译:这项工作描述了壳聚糖微针贴剂的制剂和评价,用于近甲酸钠递送Meloxicam以管理牛的疼痛。对壳聚糖和壳聚糖/美洛昔康组成的微针补丁关于其化学成分,物理特性的均匀性,渗透皮肤的能力,以及对热和热机械变化的响应。通过改变溶液制剂期间使用的乙酸的百分比来制备微针贴剂,其中包括90%(v / v),50%(v / v)和10%(v / v)。此外,通过将不同百分比的渗透到皮肤和微针贴片上的微针数进行评估,评估药物释放。扫描电子显微镜证实存在在贴片表面上均匀地组织的微酮的存在,用于使用每种乙酸的含量。傅里叶变换红外光谱显示,溶液中的10%(v / v)乙酸是一种适当的条件,以保持壳聚糖(酰胺I和酰胺II)和美洛昔康(胺Neh Stray和C = O伸展)的特征条件与溶液制备期间使用的90%(v / v)和50%(v / v)相比。得到的微针贴片成功渗透在牛的尸体耳中的皮肤。结果表明,完全脱水后测量的渗透皮肤的平均深度渗透率约为78 +/-1μm。随着温度的增加,壳聚糖和壳聚糖/含壳聚糖/美洛昔康微针贴片反射较高的抗压力抗压力。 COMSOL的稀释物种运输的时间依赖性模拟显示,透皮药物输送在表面贴片上的微针数量的递增和每微小渗透的百分比上增加。一个贴剂在每周皮肤中释放出3.57×10(-5)mol / m(3)的药物浓度,这代表牛疼痛管理所需的26.2%,建立为1.43 x 10(-4) mol / m(3)。这些结果表明,壳聚糖/美洛昔康微针贴剂可能适合于在常规程序后管理牛的疼痛。

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