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Volume 6, Issue 1
Preparation and Characterization of DHAD/HRP Co-loaded Multivesicular Liposomes

Yuangang Liu, Qiyao Zheng, Shibin Wang, Kejing Wu & Aizheng Chen

Journal of Fiber Bioengineering & Informatics, 6 (2013), pp. 95-102.

Published online: 2013-06

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  • Abstract
The structure of carriers play an important role in the space distribution of different drugs, therefore this paper studies multivesicular liposomes (MVLs), which have a unique nano-in-micro structure as possible carriers in combination therapy. Horseradish peroxidase (HRP) and mitoxantrone hydrochloride (DHAD) were selected as model drugs for protein and small molecule drug respectively. The results show that the MVLs are spherical and that the internal space is divided up into numerous compartments. The particle size ranged from 15 to 20 μm and the system was stable according to the zeta potentials. In vitro release studies display that the DHAD/HRP co-loaded MVLs has better sustained release profiles than one drug alone, and the MVLs exhibited an orderly release behavior which suggested that MVLs might be used as drug carriers in combination therapy applications.
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@Article{JFBI-6-95, author = {Yuangang Liu, Qiyao Zheng, Shibin Wang, Kejing Wu and Aizheng Chen}, title = {Preparation and Characterization of DHAD/HRP Co-loaded Multivesicular Liposomes}, journal = {Journal of Fiber Bioengineering and Informatics}, year = {2013}, volume = {6}, number = {1}, pages = {95--102}, abstract = {The structure of carriers play an important role in the space distribution of different drugs, therefore this paper studies multivesicular liposomes (MVLs), which have a unique nano-in-micro structure as possible carriers in combination therapy. Horseradish peroxidase (HRP) and mitoxantrone hydrochloride (DHAD) were selected as model drugs for protein and small molecule drug respectively. The results show that the MVLs are spherical and that the internal space is divided up into numerous compartments. The particle size ranged from 15 to 20 μm and the system was stable according to the zeta potentials. In vitro release studies display that the DHAD/HRP co-loaded MVLs has better sustained release profiles than one drug alone, and the MVLs exhibited an orderly release behavior which suggested that MVLs might be used as drug carriers in combination therapy applications.}, issn = {2617-8699}, doi = {https://doi.org/10.3993/jfbi03201309}, url = {http://global-sci.org/intro/article_detail/jfbi/4825.html} }
TY - JOUR T1 - Preparation and Characterization of DHAD/HRP Co-loaded Multivesicular Liposomes AU - Yuangang Liu, Qiyao Zheng, Shibin Wang, Kejing Wu & Aizheng Chen JO - Journal of Fiber Bioengineering and Informatics VL - 1 SP - 95 EP - 102 PY - 2013 DA - 2013/06 SN - 6 DO - http://doi.org/10.3993/jfbi03201309 UR - https://global-sci.org/intro/article_detail/jfbi/4825.html KW - Multivesicular Liposomes (MVLs) KW - Combination Therapy KW - Protein KW - Small Molecule Drug AB - The structure of carriers play an important role in the space distribution of different drugs, therefore this paper studies multivesicular liposomes (MVLs), which have a unique nano-in-micro structure as possible carriers in combination therapy. Horseradish peroxidase (HRP) and mitoxantrone hydrochloride (DHAD) were selected as model drugs for protein and small molecule drug respectively. The results show that the MVLs are spherical and that the internal space is divided up into numerous compartments. The particle size ranged from 15 to 20 μm and the system was stable according to the zeta potentials. In vitro release studies display that the DHAD/HRP co-loaded MVLs has better sustained release profiles than one drug alone, and the MVLs exhibited an orderly release behavior which suggested that MVLs might be used as drug carriers in combination therapy applications.
Yuangang Liu, Qiyao Zheng, Shibin Wang, Kejing Wu and Aizheng Chen. (2013). Preparation and Characterization of DHAD/HRP Co-loaded Multivesicular Liposomes. Journal of Fiber Bioengineering and Informatics. 6 (1). 95-102. doi:10.3993/jfbi03201309
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