Prolonged exposure of colon cancer cells to 5-fluorouracil nanoparticles improves its anticancer activity

被引:42
作者
Tawfik, Essam [1 ,2 ]
Ahamed, Maqusood
Almalik, Abdulaziz [1 ,2 ]
Alfaqeeh, Mohammad [2 ]
Alshamsan, Aws [1 ,2 ,3 ]
机构
[1] King Saud Univ, Dept Pharmaceut, Coll Pharm, Nanomed Res Unit, POB 2457, Riyadh 11451, Saudi Arabia
[2] King Abdulaziz City Sci & Technol, Life Sci & Environm Res Inst, Riyadh, Saudi Arabia
[3] King Saud Univ, King Abdullah Inst Nanotechnol, Riyadh, Saudi Arabia
关键词
5-Fluorouracil; Nanoparticles; Colon cancer; PLGA; Drug delivery; DRUG-DELIVERY; NANOPRECIPITATION METHOD; PLGA NANOPARTICLES; COLORECTAL-CANCER; RESISTANCE; TOXICITY; CHEMOTHERAPY; DEGRADATION; CARRIER; ACID);
D O I
10.1016/j.jsps.2016.05.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this study, we aimed to improve the anticancer effect of 5-FU on human colon cancer cell lines by incorporating in poly(D,L lactic-co-glycolic acid) (PLGA) nanoparticles (NPs). The 5-FU-PLGA NPs were prepared by nanoprecipitation technique. Prepared NPs were moderately dispersed with an average diameter of 133 +/- 25.19 nm. Scanning Electron Microscope (SEM) images revealed spherical structures with subtle surface irregularity. Free 5-FU dose-response curves were constructed (12.5-2000 mu M) using MTT assay on HCT 116 and HT-29 cell lines for 1,3, and 5 days. The calculated IC50 on HCT 116 were 185 mu M after 1 day, 11.3 mu M after 3 days, and 1.48 mu M after 5 days. On HT-29, IC50 was only reached after 5 days of 5-FU treatment (11.25 mu M). The HCT 116 viability following treatment with 100 mu M 5-FU in free or NPs forms for 3 days was 38.8% and 18.6%, respectively. Similarly, when 250 mu M was applied, HCT 116 viability was 17.03% and 14.6% after treatment with free and NPs forms of 5-FU, respectively. Moreover, HT-29 cell viability after 250 mu M 5-FU treatment in free or NPs forms was 55.45% and 34.01%, respectively. We also noticed that HCT 116 cells were more sensitive to 5-FU-PLGA NPs as compared to HT-29 cells. Overall, our data indicate that 5-FU activity is time dependent and the prolonged effects created by PLGA NPs may contribute, at least in part, to the noticed enhancement of the anticancer activity of 5-FU drug. (C) 2016 The Authors.
引用
收藏
页码:206 / 213
页数:8
相关论文
共 37 条
[1]   Validated High-Performance Liquid Chromatographic Technique for Determination of 5-Fluorouracil: Applications to Stability Studies and Simulated Colonic Media [J].
Alanazi, Fars K. ;
Yassin, Alaa Eldeen ;
El-Badry, Mahmoud ;
Mowafy, Hammam A. ;
Alsarra, Ibrahim A. .
JOURNAL OF CHROMATOGRAPHIC SCIENCE, 2009, 47 (07) :558-563
[2]   Advances in Nano Drugs for Cancer Chemotherapy [J].
Ali, I. ;
Rahis-Uddin ;
Salim, K. ;
Rajora, A. K. ;
Rather, M. A. ;
Wani, W. A. ;
Haque, A. .
CURRENT CANCER DRUG TARGETS, 2011, 11 (02) :135-146
[3]  
American Cancer Society, 2006, AM CANC SOC COMPL GU
[4]   Biodegradation and biocompatibility of PLA and PLGA microspheres [J].
Anderson, JM ;
Shive, MS .
ADVANCED DRUG DELIVERY REVIEWS, 1997, 28 (01) :5-24
[5]   Novel Strategies to Improve the Anticancer Action of 5-Fluorouracil by Using Drug Delivery Systems [J].
Arias, Jose L. .
MOLECULES, 2008, 13 (10) :2340-2369
[6]   Dual drug delivery of 5-fluorouracil (5-FU) and methotrexate (MTX) through random copolymeric nanomicelles of PLGA and polyethylenimine demonstrating enhanced cell uptake and cytotoxicity [J].
Ashwanikumar, N. ;
Kumar, Nisha Asok ;
Nair, S. Asha ;
Kumar, G. S. Vinod .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2014, 122 :520-528
[7]  
Avgoustakis Konstantinos, 2004, Current Drug Delivery, V1, P321, DOI 10.2174/1567201043334605
[8]   Encapsulation of hydrophilic and lipophilic drugs in PLGA nanoparticles by the nanoprecipitation method [J].
Barichello, JM ;
Morishita, M ;
Takayama, K ;
Nagai, T .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1999, 25 (04) :471-476
[9]  
Blanke CD, 1999, ONCOLOGY-NY, V13, P47
[10]   Enhanced liver targeting of 5-fluorouracil using galactosylated human serum albumin as a carrier molecule [J].
Cai, C ;
Zhou, KY ;
Wu, Y ;
Wu, LY .
JOURNAL OF DRUG TARGETING, 2006, 14 (02) :55-61