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  4. Cytotoxicity and cellular uptake capacity of a berberine-loaded nanogold/collagen drug delivery system in lung cancer
 
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Cytotoxicity and cellular uptake capacity of a berberine-loaded nanogold/collagen drug delivery system in lung cancer

Journal
Colloids and Surfaces A: Physicochemical and Engineering Aspects
Journal Volume
702
Start Page
134961
ISSN
0927-7757
Date Issued
2024-12-05
Author(s)
Chien-Lun Tang
Chen-Feng Chiu
SHAN-HUI HSU  
Song-Yi Yan
Chun-Yu Yueh
Gregory J. Tsay
Wen-Ching Chiu
Yi-Chin Yang
Alex Yang-Hao Yu
Huey-Shan Hung
DOI
10.1016/j.colsurfa.2024.134961
DOI
10.1016/j.colsurfa.2024.134961
URI
https://www.scopus.com/record/display.uri?eid=2-s2.0-85200817753&origin=resultslist
https://scholars.lib.ntu.edu.tw/handle/123456789/720405
Abstract
Lung cancer is the leading cause of cancer-related deaths worldwide. As an emerging technology, nanomedicine offers a more effective and biocompatible approach to treating lung cancer by targeting and killing uncontrolled cancer cells. This study fabricated a nanocarrier system comprising gold nanoparticles, type I collagen, and alkaline berberine (Au-Col-BB). It then thoroughly evaluated the physical and biological properties of this novel drug delivery system. The material properties were characterized using UV-Vis spectroscopy, Fourier-transform infrared spectroscopy, scanning electron microscopy, dynamic light scattering, energy-dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy. MTT and Calcein AM staining of A549 lung cancer cells demonstrated that treatment with Au-Col-BB significantly decreased cell viability. Annexin V/propidium iodide double staining and cell cycle progression revealed that treatment with Au-Col-BB increased apoptosis 1.82-fold in A549 cells but decreased apoptosis 0.94-cold in BEAS-2B normal lung cells. The percentage of A549 cells in the sub-G1 phase increased from 4.0 % to 11.6 % (p < 0.001), while the percentage of those in the S phase decreased from 14.5 % to 9.6 % (p < 0.010), indicating enhanced apoptosis and reduced proliferation. Treatment with Au-Col-BB significantly reduced the migration distance of A549 cells by 51 %. Au-Col-BB was found to primarily enter cells via clathrin-mediated endocytosis and autophagy, which were inhibited by chlorpromazine and bafilomycin A1, respectively. Retroorbital sinus injection of Au-Col-BB into BALB/c mice demonstrated its integrity and safety in vivo. Overall, this study suggests that the Au-Col-BB nanocarrier system is a promising alternative for antineoplastic drugs, offering effective cancer cell targeting and apoptosis induction while minimizing damage to surrounding healthy tissues.
Subjects
Berberine
Cell autophagy
Clathrin-mediated endocytosis
Endocytosis
Gold nanoparticles
Lung cancer
Type I collagen
SDGs

[SDGs]SDG3

Publisher
Elsevier BV
Type
journal article

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