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Preparation of ropivacaine loaded PLGA microspheres as controlled-release system with narrow size distribution and high loading efficiency
Li, Xun1,2; Wei, Yi1; Lv, Piping1; Wu, Youbin3; Ogino, Kenji4; Ma, Guanghui1
2019-02-05
Source PublicationCOLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
ISSN0927-7757
Volume562Pages:237-246
AbstractRopivacaine loaded microspheres offer an attractive alternative for prolonging the duration of local anesthetics for the pain management. However, traditional microcapsulation methods could not provide microspheres with desired drug loading efficiency and a narrow size distribution, leading to poor patient compliance as well as preparation repeatability. In this study, we proposed to combine O/W emulsion method with novel premix membrane emulsification technique. After the optimization of fabrication procedure, ropivacaine loaded microspheres with narrow size distribution (span 0.469), high drug loading efficiency (49%) and an ideal constant release behavior have been obtained. Especially, it was found that solidification process affected the internal structure of microspheres and the physical state of encapsulated ropivacaine. Furthermore, it was interested that lower polymer molecular weight resulted in higher encapsulation efficiency, which was not consistent with reported results. It was found that this was ascribed to the interaction of PLGA-ropivacaine. All these aspects had considerable influences on the characteristics of microspheres. In addition, the cytotoxicity on different cell lines (SHSY5Y and HaCaT cells) was detected qualitatively and quantitatively. It showed that ropivacaine loaded microspheres did reduce the Reactive oxygen species (ROS) and cytotoxicity prominently compared to free ropivacaine, which could be attributed to the sustained and steady drug release behavior. This study provided some pioneering ideas for encapsulating small molecule drug with poor solubility. The optimized microspheres could be chosen as an ideal candidate for the ropivacaine sustained release with its better drug adherence, lower toxicity of drug burst release and best therapeutic effect.
KeywordRopivacaine PLGA microsphere High drug loading Narrow size distribution Reduce cytotoxicity
DOI10.1016/j.colsurfa.2018.11.014
Language英语
WOS KeywordBUPIVACAINE ; FORMULATION ; EFFICACY ; ENCAPSULATION ; CYTOTOXICITY ; PARTICLES ; APOPTOSIS ; STRATEGY ; DELIVERY ; DRUGS
Funding ProjectNational Nature Science Foundation of China[21336010] ; National Key Technology Program[2017ZX09201004014]
WOS Research AreaChemistry
WOS SubjectChemistry, Physical
Funding OrganizationNational Nature Science Foundation of China ; National Key Technology Program
WOS IDWOS:000454428500029
PublisherELSEVIER SCIENCE BV
Citation statistics
Document Type期刊论文
Identifierhttp://ir.ipe.ac.cn/handle/122111/27654
Collection中国科学院过程工程研究所
Corresponding AuthorWei, Yi; Ma, Guanghui
Affiliation1.Chinese Acad Sci, Inst Proc Engn, State Key Lab Biochem Engn, PLA Key Lab Biopharmaceut Prod & Formulat Engn, Beijing 100190, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
3.Yichang Humanwell Pharmaceut Co Ltd, Yichang 443008, Peoples R China
4.Tokyo Univ Agr & Technol, Grad Sch Bioapplicat Syst Engn, Koganei, Tokyo 1848588, Japan
Recommended Citation
GB/T 7714
Li, Xun,Wei, Yi,Lv, Piping,et al. Preparation of ropivacaine loaded PLGA microspheres as controlled-release system with narrow size distribution and high loading efficiency[J]. COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,2019,562:237-246.
APA Li, Xun,Wei, Yi,Lv, Piping,Wu, Youbin,Ogino, Kenji,&Ma, Guanghui.(2019).Preparation of ropivacaine loaded PLGA microspheres as controlled-release system with narrow size distribution and high loading efficiency.COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,562,237-246.
MLA Li, Xun,et al."Preparation of ropivacaine loaded PLGA microspheres as controlled-release system with narrow size distribution and high loading efficiency".COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS 562(2019):237-246.
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