Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Xuezhi Zhuo"'
Autor:
Xuezhi Zhuo, Maud Margrethe Brekstad Kjellin, Zarah Schaal, Tengyu Zhang, Korbinian Löbmann, Donglei Leng
Publikováno v:
Pharmaceutics, Vol 15, Iss 1, p 126 (2022)
Amorphous solid dispersions (ASDs) based on proteins as co-formers have previously shown promising potential to improve the solubility and bioavailability of poorly water-soluble drugs. In particular, whey proteins have shown to be promising co-forme
Externí odkaz:
https://doaj.org/article/468e59b7884941d0b6e951dacb38b72d
Autor:
Aleksei Kabedev, Xuezhi Zhuo, Donglei Leng, Vito Foderà, Min Zhao, Per Larsson, Christel A. S. Bergström, Korbinian Löbmann
Publikováno v:
Kabedev, A, Zhuo, X, Leng, D, Foderà, V, Zhao, M, Larsson, P, Bergström, C A S & Löbmann, K 2022, ' Stabilizing mechanisms of β-lactoglobulin in amorphous solid dispersions of indomethacin ', Molecular Pharmaceutics, vol. 19, no. 11, pp. 3922-3933 . https://doi.org/10.1021/acs.molpharmaceut.2c00397
Kabedev, A, Zhuo, X, Leng, D, Foderà, V, Zhao, M, Larsson, P, Bergström, C A S & Löbmann, K 2022, ' Stabilizing Mechanisms of β-Lactoglobulin in Amorphous Solid Dispersions of Indomethacin ', Molecular Pharmaceutics, vol. 19, no. 11, pp. 3922–3933 . https://doi.org/10.1021/acs.molpharmaceut.2c00397
Kabedev, A, Zhuo, X, Leng, D, Foderà, V, Zhao, M, Larsson, P, Bergström, C A S & Löbmann, K 2022, ' Stabilizing Mechanisms of β-Lactoglobulin in Amorphous Solid Dispersions of Indomethacin ', Molecular Pharmaceutics, vol. 19, no. 11, pp. 3922–3933 . https://doi.org/10.1021/acs.molpharmaceut.2c00397
Proteins, and in particular whey proteins, have recently been introduced as a promising excipient class for stabilizing amorphous solid dispersions. However, despite the efficacy of the approach, the molecular mechanisms behind the stabilization of t
Autor:
Yu Zhang, Tian Yin, Linlin Miao, Yihan Kong, Jia Su, Haibing He, Xuezhi Zhuo, Jingxin Gou, Xing Tang, Lifeng Luo
Publikováno v:
Molecular Pharmaceutics. 15:1556-1564
The clinical application of disulfiram (DSF) in cancer treatments is hindered by its rapid degradation in the blood circulation. In this study, methoxy poly(ethylene glycol)-b-poly(lactide-co-glycolide)/poly(e-caprolactone) (mPEG5k-b-PLGA2k/PCL3.4k)
Autor:
Lu Liu, Haibing He, Qiuyue Chen, Xiuzhi Wang, Tian Yin, Lifeng Luo, Xing Tang, Linlin Miao, Yu Zhang, Xuezhi Zhuo, Jiawen Xu
Publikováno v:
European Journal of Pharmaceutical Sciences. 109:638-649
The purpose of the study was to develop a parenteral docetaxel lipid microsphere to inhibit its 7-epidocetaxel conversion in vitro and in vivo. 7-epidocetaxel conversion as the main indicator was investigated to optimize the formulation and process.
Publikováno v:
International Journal of Pharmaceutics. 528:62-75
A series of mixed hydrogels of PLGA-PEG-PLGA and PCLA-PEG-PCLA were synthesized, and investigated in terms of their critical micelle concentration, stability and thermosensitive properties. Also, some mixed hydrogel was selected to prepare Depot-gel-
Autor:
Jingxin Gou, Haibing He, Xing Tang, Xuezhi Zhuo, Tianyang Ren, Wei Chu, Puxiu Wang, Tian Yin, Yu Zhang
Publikováno v:
Journal of Materials Chemistry B. 5:1551-1565
PLGA-PEG-PLGA (PPP) triblock copolymer is the most widely studied thermosensitive hydrogel owing to its non-toxic, biocompatible, biodegradable, and thermosensitive properties. PPP thermosensitive hydrogels are being investigated as in situ gels beca
Autor:
Qing Cai, Xing Tang, Xuezhi Zhuo, Jingxin Gou, Tian Yin, Pengqian Tian, Haibing He, Yu Zhang, Zhaohui Tang, Wei Chu, Jinlong Li, Ning Ding
Publikováno v:
Pharmaceutical research. 35(12)
Despite being widely used for the treatment of several solid tumors, Gemcitabine (GEM) exhibits several suboptimal pharmacokinetic properties. Therefore, the design of nanoparticle delivery systems is a promising strategy to enhance GEM pharmacokinet
Autor:
Linlin, Miao, Jia, Su, Xuezhi, Zhuo, Lifeng, Luo, Yihan, Kong, Jingxin, Gou, Tian, Yin, Yu, Zhang, Haibing, He, Xing, Tang
Publikováno v:
Molecular pharmaceutics. 15(4)
The clinical application of disulfiram (DSF) in cancer treatments is hindered by its rapid degradation in the blood circulation. In this study, methoxy poly(ethylene glycol)- b-poly(lactide- co-glycolide)/poly(ε-caprolactone) (mPEG
Autor:
Jingxin Gou, Wei Chu, Xing Tang, Xuezhi Zhuo, Linlin Miao, Lifeng Luo, Haibing He, Xiaowen Li, Tian Yin, Yu Zhang, Tian Lei
Publikováno v:
Journal of colloid and interface science. 529
To develop an injectable formulation and improve the stability of disulfiram (DSF), DSF was encapsulated into mixed nanoparticles (DSF-NPs) through a high-pressure homogenization method. The Flory-Huggins interaction parameters (χFH) were calculated
Autor:
Zhuo, Xuezhi1 (AUTHOR), Margrethe Brekstad Kjellin, Maud1 (AUTHOR), Schaal, Zarah1 (AUTHOR), Zhang, Tengyu1 (AUTHOR), Löbmann, Korbinian1,2 (AUTHOR), Leng, Donglei2 (AUTHOR) dl@zerion.eu
Publikováno v:
Pharmaceutics. Jan2023, Vol. 15 Issue 1, p126. 10p.