Polyacrylamide-punicic acid conjugate-based micelles for flutamide delivery in PC3 cells of prostate cancer: synthesis, characterisation and cytotoxicity studies

(2020) Polyacrylamide-punicic acid conjugate-based micelles for flutamide delivery in PC3 cells of prostate cancer: synthesis, characterisation and cytotoxicity studies. Iet Nanobiotechnology. pp. 417-422. ISSN 1751-8741

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Abstract

The aim of the present study was to synthesize a novel biopolymeric micelle based on punicic acid (PA) and polyacrylamide (PAM) for carrying chemotherapeutic drugs used in prostate cancer treatment. A polymer composite micelle was prepared by chemical conjugation between PAM and PA. The micelles were prepared by self-assembly via film casting followed by ultrasonication method. The successful production of PAMPA copolymeric micelles was confirmed using FTIR, 1H-NMR, and TEM. Then, flutamide was loaded in the designed nanomicelles and they were characterized. The cell cytotoxicity of the micelles was studied on PC3 cells of prostate cancer. The prepared nanomicelles showed the particle size of 88 nm, PDI of 0.246, zeta potential of -9 mV, drug loading efficiency of 94.5, drug release of 85.6 until 10 hours in pH 7.4 and CMC of 74.13 mu g/ml. The cell viability in blank nanocarriers was about 70 in PC3 cells at concentration of 25 mu M. More significant cytotoxic effects were seen for flutamide loaded micelles at this concentration compared to the free drug. The results suggest that the PAMPA co-polymeric nanomicelles can be utilized as an effective carrier to enhance the cytotoxic effects of flutamide in prostate cancer.

Item Type: Article
Keywords: nanoparticles cellular biophysics drugs biomedical materials drug delivery systems colloids hydrophilicity pH transmission electron microscopy particle size cancer casting toxicology electrokinetic effects polymer blends proton magnetic resonance nanomedicine self-assembly nanofabrication Fourier transform infrared spectra PC3 cells chemotherapeutic drugs prostate cancer treatment polymer composite micelle chemical conjugation proton nuclear magnetic resonance cell cytotoxicity prepared nanomicelles drug loading efficiency drug release critical micelle concentration cell viability cytotoxic effects flutamideloaded micelles flutamide delivery polyacrylamide-punicic acid conjugate-based micelles PAMPA copolymeric nanomicelles biopolymeric micelle PAM-punicic acid copolymer copolymeric micelles hydrophilic shell self-assembly film casting ultrasonication method Fourier transform infrared spectra transmission electron microscopy particle size polydisperity index zeta potential pH blank nanocarriers time 10 0 hour POLYMERIC MICELLES DRUG-DELIVERY POMEGRANATE JUICE NANOPARTICLES RELEASE NANOCARRIERS THERAPY CHEMOPREVENTION INHIBITION COPOLYMER
Subjects: QV Pharmacology
QZ Pathology > QZ 200-380 Neoplasms
WJ Urogenital System > WJ 700-875 Male Genitalia
Divisions: Faculty of Pharmacy and Pharmaceutical Sciences > Department of Pharmacotherapy
Novel Drug Delivery Systems Research Center
Page Range: pp. 417-422
Journal or Publication Title: Iet Nanobiotechnology
Journal Index: ISI
Volume: 14
Number: 5
Identification Number: https://doi.org/10.1049/iet-nbt.2020.0014
ISSN: 1751-8741
Depositing User: Zahra Otroj
URI: http://eprints.mui.ac.ir/id/eprint/13141

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