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Preparation and in vitro evaluation of FGF-2 incorporated carboxymethyl chitosan nanoparticles

Nguyen C.-T. Department of Molecular and Environmental Biotechnology, Falcuty of Biology and Biotechnology, Viet Nam|
Tran-Van H. | Tran L.T. | Nguyen A.D. | Nguyen P.P.T. | Nguyen T.-T. Institute of Biotechnology and Enviroment, Tay Nguyen University, Buon Ma Thuot, Viet Nam| Nguyen T.-T. Department of Physical Chemistry, Faculty of Chemistry, University of Science, Vietnam National University, Ho Chi Minh City, Viet Nam|

Carbohydrate Polymers Số , năm 2017 (Tập 173, trang 114-120)

ISSN: 1448617

ISSN: 1448617

DOI: 10.1016/j.carbpol.2017.05.080

Tài liệu thuộc danh mục: Scopus

Article

English

Từ khóa: Cell culture; Chitin; Chitosan; Crosslinking; Gelation; Nanoparticles; Proteins; Carboxylmethyl chitosan; Carboxymethyl chitosan; Cross-linking reagents; Drug release; FGF-2; Fibroblast growth factor 2; In-vitro evaluation; Ionic gelations; Synthesis (chemical)
Tóm tắt tiếng anh
Fibroblast growth factor 2 (FGF-2) is a multi-functional protein involving in wound healing. However, FGF-2 is easily degradable in vivo, which limited its use for wound treatment. In this study, we investigated a drug-delivery model for FGF-2 via incorporation with biodegradable carboxylmethyl chitosan (CMCS). CMCS nanoparticles (NPs) could be synthesized by ionic gelation using CaCl2 as a crosslinking reagent with the CMCS:CaCl2 ratio of 1:0.8. Synthesized CMCS NPs had a diameter of 32.68 ± 6.83 nm, and were non-toxic at concentrations up to 2.5 mg/ml. Incorporated CMCS:FGF‐2 NPs had a diameter of 34.83 ± 5.89 nm and incorporation efficiency was 95%. CMCS:FGF‐2 NPs released 36.36% and 58.47% of FGF‐2 after 48 h incubation in two different pH of 7.4 and 5.8, respectively. The incorporation and release processes did not have a significant effect on FGF-2 activity. Simultaneously, CMCS:FGF-2 NPs could protect FGF‐2 from the degradation of trypsin in vitro. Our results laid the groundwork for the manufacturing of protein incorporated CMCS NPs for bio‐applications. © 2017 Elsevier Ltd

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