Literature DB >> 23518367

Preparation and characterization of galactosylated bovine serum albumin nanoparticles for liver-targeted delivery of oridonin.

Caiyun Li1, Dianrui Zhang, Hejian Guo, Leilei Hao, Dandan Zheng, Guangpu Liu, Jingyi Shen, Xiaona Tian, Qiang Zhang.   

Abstract

In this study, galactosylated bovine serum albumin (GB), which could be developed for a liver targeting carrier was synthetized and it was identified by Fourier transform infrared (FT-IR) spectrometer. Oridonin loaded bovine serum albumin nanoparticle (ORI-BSA-NP) and oridonin loaded GB nanoparticle (ORI-GB-NP) were prepared and optimized by the desolvation technique. During the preparation of ORI-GB-NP, galactosamine was introduced to end-cap the free aldehyde groups on nanoparticles. The characteristics of ORI-GB-NP such as particle size, zeta potential, particle morphologie, entrapment efficiency and drug loading were evaluated. The nearly spherical nanoparticles, with a narrow size distribution below 200 nm, were negatively charged with zeta potential of about -30 mV. Meanwhile, differential scanning calorimetry (DSC) and X-ray diffraction confirmed the amorphous state of ORI in ORI-GB-NP. The in vitro drug release of ORI from ORI-GB-NP presented a biphasic pattern with an initial burst effect and consequently sustained release. These results implied that the nanoparticles possessed fine physicochemical characteristics and seemed to be a stable delivery system for poorly soluble oridonin.
Copyright © 2013 Elsevier B.V. All rights reserved.

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Year:  2013        PMID: 23518367     DOI: 10.1016/j.ijpharm.2013.03.019

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  13 in total

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Authors:  Lifei Zhu; Miao Li; Xiaoyan Liu; Lina Du; Yiguang Jin
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10.  Curcumin-loaded galactosylated BSA nanoparticles as targeted drug delivery carriers inhibit hepatocellular carcinoma cell proliferation and migration.

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