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학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
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연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2021.3
- 수록면
- 228 - 235 (8page)
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초록· 키워드
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Backgroud: Ginsenoside compound K (GK) is a major metabolite of protopanaxadiol-type ginsenosides and has remarkable anticancer activities in vitro and in vivo. This work used an ionic cross-linking method to entrap GK within O-carboxymethyl chitosan (OCMC) nanoparticles (Nps) to form GK-loaded OCMC Nps (GK―OCMC Nps), which enhance the aqueous solubility and stability of GK.
Methods: The GK―OCMC Nps were characterized using several physicochemical techniques, including x-ray diffraction, transmission electron microscopy, zeta potential analysis, and particle size analysis via dynamic light scattering. GK was released from GK―OCMC Nps and was conducted using the dialysis bag diffusion method. The effects of GK and GK―OCMC Nps on PC3 cell viability were measured by using the 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide assay. Fluorescent technology based on Cy5.5-labeled probes was used to explore the cellular uptake of GK―OCMC Nps.
Results: The GK―OCMC NPs had a suitable particle size and zeta potential; they were spherical with good dispersion. In vitro drug release from GK―OCMC NPs was pH dependent. Moreover, the in vitro cytotoxicity study and cellular uptake assays indicated that the GK―OCMC Nps significantly enhanced the cytotoxicity and cellular uptake of GK toward the PC3 cells. GK―OCMC Nps also significantly promoted the activities of both caspase-3 and caspase-9.
Conclusion: GK―OCMC Nps are potential nanocarriers for delivering hydrophobic drugs, thereby enhancing water solubility and permeability and improving the antiproliferative effects of GK.
Methods: The GK―OCMC Nps were characterized using several physicochemical techniques, including x-ray diffraction, transmission electron microscopy, zeta potential analysis, and particle size analysis via dynamic light scattering. GK was released from GK―OCMC Nps and was conducted using the dialysis bag diffusion method. The effects of GK and GK―OCMC Nps on PC3 cell viability were measured by using the 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide assay. Fluorescent technology based on Cy5.5-labeled probes was used to explore the cellular uptake of GK―OCMC Nps.
Results: The GK―OCMC NPs had a suitable particle size and zeta potential; they were spherical with good dispersion. In vitro drug release from GK―OCMC NPs was pH dependent. Moreover, the in vitro cytotoxicity study and cellular uptake assays indicated that the GK―OCMC Nps significantly enhanced the cytotoxicity and cellular uptake of GK toward the PC3 cells. GK―OCMC Nps also significantly promoted the activities of both caspase-3 and caspase-9.
Conclusion: GK―OCMC Nps are potential nanocarriers for delivering hydrophobic drugs, thereby enhancing water solubility and permeability and improving the antiproliferative effects of GK.
목차
ABSTRACT
1. Introduction
2. Materials and methods
3. Results and discussion
4. Conclusion
References
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