Pathak Shiva, Gupta Biki, Poudel Bijay Kumar, Tran Tuan Hiep, Regmi Shobha, Pham Tung Thanh, Thapa Raj Kumar, Kim Min-Soo, Yong Chul Soon, Kim Jong Oh, Jeong Jee-Heon
College of Pharmacy, Yeungnam University.
Chem Pharm Bull (Tokyo). 2016;64(2):171-8. doi: 10.1248/cpb.c15-00799.
Tacrolimus-loaded poly(lactic-co-glycolic acid) microspheres (TAC-PLGA-M) can be administered for the long-term survival of transplanted organs due to their immunosuppressive activity. The purpose of our study was to optimize the parameters of the electrospray method, and to prepare TAC-PLGA-M with a high payload and desirable release properties. TAC-PLGA-M were prepared using the electrospray method. In vitro characterization and evaluation were performed using scanning electron microscopy, X-ray diffraction (XRD), differential scanning calorimetry (DSC), and Fourier-transform infrared spectroscopy. Drug-loading efficiency was greater than 80% in all formulations with a maximum loading capacity of 16.81±0.37%. XRD and DSC studies suggested that the drug was incorporated in an amorphous state or was molecularly dispersed in the microspheres. The in vitro release study showed prolonged release patterns. TAC-PLGA-M with enhanced drug loading and prolonged-release patterns were successfully prepared using the electrospray method.
负载他克莫司的聚乳酸-羟基乙酸共聚物微球(TAC-PLGA-M)因其免疫抑制活性可用于移植器官的长期存活。本研究的目的是优化电喷雾法的参数,并制备具有高载药量和理想释放特性的TAC-PLGA-M。采用电喷雾法制备TAC-PLGA-M。使用扫描电子显微镜、X射线衍射(XRD)、差示扫描量热法(DSC)和傅里叶变换红外光谱进行体外表征和评估。所有制剂的载药效率均大于80%,最大载药量为16.81±0.37%。XRD和DSC研究表明,药物以无定形状态掺入或分子分散在微球中。体外释放研究显示出延长的释放模式。采用电喷雾法成功制备了载药量增加且具有延长释放模式的TAC-PLGA-M。