| Literature DB >> 25951620 |
Xiaozhou Huang1, Na Li2, Dajiang Wang3, Yuyan Luo1, Ziyu Wu4, Zhefei Guo1, Qixing Jin1, Zhuying Liu1, Yafei Huang1, Yongming Zhang5, Chuanbin Wu6.
Abstract
The objective of this study was to investigate the use of transmission hard X-ray nano-computed-tomography (nano-CT) for characterization of the pore structure and drug distribution in poly (lactic-co-glycolic acid) (PLGA) microspheres encapsulating bovine serum albumin and to study the correlation between drug distribution and burst release. The PLGA microspheres were fabricated using a double-emulsion method. The results of pore structure analysis accessed with nano-CT were compared with those acquired by scanning electron microscopy (SEM) and confocal laser scanning microscopy (CLSM). Surface pore interconnectivity and surface protein interconnectivity were obtained using combined nano-CT and pixel analysis. The correlation between surface protein interconnectivity with the initial burst release across various tested formulations was also analyzed. The size, shape, and distribution of the pores and protein could be clearly observed in the whole microsphere using nano-CT, whereas only the sectional information was observed using SEM or CLSM. Interconnected pores and surface connected pores could be clearly distinguished in nano-CT, which enables the quantitative analysis of surface pore interconnectivity and surface protein interconnectivity. The surface protein interconnectivity in different formulations correlated well with the burst release at 5-10h. Nano-CT provided a nondestructive, high-resolution, and three-dimensional analysis method to characterize the porous microsphere.Entities:
Keywords: PLGA microspheres; Pore structure; Scanning electron microscopy (SEM); Surface protein interconnectivity; Transmission hard X-ray nano-tomography (nano-CT)
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Year: 2015 PMID: 25951620 DOI: 10.1016/j.jpba.2015.04.017
Source DB: PubMed Journal: J Pharm Biomed Anal ISSN: 0731-7085 Impact factor: 3.935