Investigation of Polyacrylic Acid Toxicity in Human Breast Cancer (MCF-7) and Mouse Fibroblast (L-929) Cell Lines

被引:1
|
作者
Ersoz, Melike [1 ]
Allahverdiyev, Adil [2 ]
机构
[1] Univ Demiroglu Bilim, Dept Mol Biol & Genet, Istanbul, Turkey
[2] Natl Medival Res Inst Prevent V Akhundov, Baku, Azerbaijan
来源
EUROBIOTECH JOURNAL | 2021年 / 5卷 / 03期
关键词
Apoptosis; biocompatibility; cytotoxicity; polyacrylic acid; CYTOTOXICITY; NANOPARTICLES; RADIATION; HYDROGELS; COATINGS; DELIVERY;
D O I
10.2478/ebtj-2021-0021
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In recent years, biopolymers have been widely used in various fields of medicine. Before using any polymer, its biocompatibility should be examined. Polyacrylic acid (PAA), a polyelectrolyte, is known to be used as an adjuvant effect in immunology, anti-thrombogenic effect in medical experiments, and as a carrier in drug delivery systems. Although there are studies on various conjugates and nanoparticles of PAA, studies on its toxicity alone are limited. Determination of toxicity in biopolymer studies is extremely important. Cultures of various cells are used for toxicity analyses. This study aimed to investigate the toxicity of PAA in human breast cancer (MCF-7) and mouse fibroblast (L-929) cell lines by various methods. Cell culture, 3-(4,5-dimethyltriazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), trypan blue and 4,6-diamidino 2 phenylindole (DAPI) methods were used in the study. The half-maximal effective concentration (EC50) value of PAA was 6.6 mg/ml in MCF 7 cells and 1.8 mg/ml in L-929 cells. Apoptosis was observed in cells on the increasing PAA concentration with DAPI. With these results, the cytotoxic properties of PAA were determined in vitro. Accordingly, the biocompatibility of polymers to be used in modeling should be supported by in vitro and in vivo studies.
引用
收藏
页码:123 / 129
页数:7
相关论文
共 50 条
  • [11] Estrogen regulation of MRP1 in MCF-7 and MCF-7/VP breast cancer cell lines.
    Odlum, AC
    Procko, K
    Dean, D
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2003, 225 : U357 - U357
  • [12] THE COVALENT LABELING OF PROTEINS BY 17-BETA-ESTRADIOL, RETINOIC ACID, AND PROGESTERONE IN THE HUMAN BREAST-CANCER CELL-LINES MCF-7 AND MCF-7/ADRR
    TAKAHASHI, N
    BREITMAN, TR
    JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1992, 43 (06): : 489 - 497
  • [13] Effect of Nerium oleander distillate on MCF-7 breast cancer cell lines
    Kars, Meltem Demirel
    Kars, Gokhan
    Gunduz, Ufuk
    Uney, Kamil
    Bas, Ahmet Levent
    CURRENT OPINION IN BIOTECHNOLOGY, 2011, 22 : S126 - S126
  • [14] Anticancer and Cytotoxic Activities of Some Trigonella Species on MCF-7, L929 and HeLa Cell Lines
    Mojarradgandoukmolla, Shahrokh
    Akan, Hasan
    Kasim, Takim
    Dastan, Sevgi Durna
    Aktas, Hatice Gumushan
    BIOLOGY BULLETIN, 2024, 51 (04) : 829 - 834
  • [15] Antimetastatic Effects of Phyllanthus on Human Lung (A549) and Breast (MCF-7) Cancer Cell Lines
    Lee, Sau Har
    Jaganath, Indu Bala
    Wang, Seok Mui
    Sekaran, Shamala Devi
    PLOS ONE, 2011, 6 (06):
  • [16] Glycosphingolipid composition of MDA-MB-231 and MCF-7 human breast cancer cell lines
    Nohara, K
    Wang, F
    Spiegel, S
    BREAST CANCER RESEARCH AND TREATMENT, 1998, 48 (02) : 149 - 157
  • [17] Glycosphingolipid composition of MDA-MB-231 and MCF-7 human breast cancer cell lines
    Keiko Nohara
    Fang Wang
    Sarah Spiegel
    Breast Cancer Research and Treatment, 1998, 48 : 149 - 157
  • [18] Methionine cytotoxicity in the human breast cancer cell line MCF-7
    Hyung H. Kim
    Chung S. Park
    In Vitro Cellular & Developmental Biology - Animal, 2003, 39 : 117 - 119
  • [19] Methionine cytotoxicity in the human breast cancer cell line MCF-7
    Kim, HH
    Park, CS
    IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL, 2003, 39 (3-4) : 117 - 119
  • [20] Retinoic acid inhibition of cell cycle progression in MCF-7 human breast cancer cells
    Zhu, WY
    Jones, CS
    Kiss, A
    Matsukuma, K
    Amin, S
    De Luca, LM
    EXPERIMENTAL CELL RESEARCH, 1997, 234 (02) : 293 - 299