Cited by 56Photodynamic Therapy Research StudiesAdvanced Drug Delivery SystemsNanoparticle-Based Drug Delivery

The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.

Colorectal cancer cell detection by 5-aminolaevulinic acid-loaded chitosan nano-particles

Yang, Shu-Jyuan, Shieh, Ming-Jium, Lin, Feng-Huei, Lou, Pei-Jen, Peng, Cheng-Liang, Wei, Ming-Feng, Yao, Cheng-Jun, Lai, Ping-Shan, Young, Tai-Horng·2009·Cancer Letters

Abstract

Colorectal cancer is one of the leading causes of malignant death in Taiwan because it often remains undetected until later stages of the disease. In this study, we designed an oral form nano-particle to encapsulate 5-aminolaevulinic acid (5-ALA) to improve the detection of colorectal cancer cells in vivo. The nano-particle should escape from bacteria uptake in the gastrointestinal tract which seriously interferes the results of endoscopic observation. In this study, chitosan was mixed with sodium tripolyphosphate (STPP) and 5-ALA to prepare chitosan nano-particles (CN) and 5-ALA loaded chitosan nano-particles (CNA) by adding different pH values and concentrations of 5-ALA solution. The average particle size and zeta-potential of CN and CNA were measured by the Zetasizer-3000. The results revealed that particle size with different zeta-potential could be manipulated just by 5-ALA concentrations and pH values. CNA particles prepared at pH 7.4 and pH 9 of 5-ALA solutions with a concentration higher than 0.5 mg/ml showed a promising loading efficiency of up to 75% and an optimum average particle size of 100 nm. The zeta-potential for CNA was over 30 mV that kept the nano-particle stable without aggregation when stored in suspension solution. Fluorescence microscope examination showed that CNA could be engulfed by Caco-2 colon cancer cells but showed no evidence of being taken up by Escherichia coli. This result implies that CNA could exclude the influence of normal flora inside the gut and serves as an adequate tool for fluorescent endoscopic detection of colorectal cancer cells in vivo.

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Crossref · 10.1016/j.canlet.2008.08.014

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  1. Mountney, 1994, Colorectal cancer, vol. 1

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Metadata

Authors
Yang, S.-J., Shieh, M.-J., Lin, F.-H., Lou, P.-J., Peng, C.-L., Wei, M.-F., Yao, C.-J., Lai, P.-S., & Young, T.-H.
Affiliations
  • National Taiwan University (TW)
  • Tao Yuan General Hospital (TW)
  • National Chung Hsing University (TW)
Corresponding author
Shieh, Ming-Jium
Venue
Cancer Letters
Publisher
Elsevier BV
Published
2009-01
Volume
273
Issue
2
Pages
210-220
ISSN
0304-3835 (ISSN-L)
OpenAlex
W2131829423
Cited by
56
References
27
Citations by year
2025: 3 · 2024: 1 · 2023: 1 · 2021: 8 · 2020: 4 · 2019: 3 · 2018: 4 · 2017: 7 · 2016: 1 · 2015: 2 · 2014: 2 · 2013: 3 · 2012: 8
FWCI
2.76
Type
journal article
Language
en
Open access
closed
Locations
  • Cancer Letters (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Science Council
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Photodynamic Therapy Research Studies
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
  • Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
Keywords
colorectal cancer, 5-aminolevulinic acid, chitosan nanoparticles, sodium tripolyphosphate, Caco-2 cells, drug loading efficiency, zeta potential
MeSH terms
Aminolevulinic Acid, Endoscopy, Escherichia coli, Humans, Hydrogen-Ion Concentration, Medical Oncology, Microscopy, Fluorescence, Particle Size, Polyphosphates, Colorectal Neoplasms, Photosensitizing Agents, Caco-2 Cells, Microscopy, Electron, Transmission, Chitosan, Nanoparticles

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