Matches in SemOpenAlex for { <https://semopenalex.org/work/W2895035716> ?p ?o ?g. }
- W2895035716 endingPage "311" @default.
- W2895035716 startingPage "301" @default.
- W2895035716 abstract "The advent of smart nanohydrogel has revealed new opportunities for scientists to develop the most efficient anti-cancer vehicles with safe and biocompatible profile. In this experiment, using reversible addition-fragmentation chain transfer polymerization method as a novel, safe and smart pH responsive formulation of poly (hydroxyethyl methacrylate-co-N,N-dimethylaminoethyl methacrylate) and poly (ethylene glycol)-diacrylate as cross-linker were synthesized. The synthesized structure was confirmed by Fourier-transform infrared spectroscopy and proton nuclear magnetic resonance methods. The pH responsive behavior of the synthesized particles was checked by size measurement in two different pH values (5.5 and 7.4) by dynamic light scattering and transmission electron microscopy. The prepared structure had nanometer sizes of 180 in medium with pH of 7.4, when it encountered acidic medium (e.g. pH 5.5), the particles swelled to about 400 nm. The efficiency of the prepared pH responsive nanohydrogels was tested as a drug delivery system. An anti-cancer drug, doxorubicin successfully interacted with this material. The release profiles of nanoparticles carrying drug molecules were checked in two different simulated pH of healthy organs (7.4) and tumor site (5.5). Despite lower release in pH of 7.4 (∼20%), an increased drug release of 80% was obtained in pH of 5.5. The in vitro toxicity assay, apoptosis evaluation and uptake experiments were performed on breast cancer cell line (MCF-7), which showed a time dependency cellular entrance, an enhanced cytotoxicity and apoptosis induction by the doxorubicin loaded nanoparticles. Hemolysis assays confirmed the safety and hemocompatibility of the developed nanohydrogel. The suitable size (<200 nm), pH responsive behavior, anti-proliferative activity and apoptosis induction in cancer cells and hemocompatibility were the noticeable features of the developed doxorubicin adsorbed nanoparticle, which introduced this formulation as an ideal vehicle in anti-cancer drug delivery." @default.
- W2895035716 created "2018-10-12" @default.
- W2895035716 creator A5015167261 @default.
- W2895035716 creator A5023838377 @default.
- W2895035716 creator A5080705836 @default.
- W2895035716 creator A5081525903 @default.
- W2895035716 date "2018-12-01" @default.
- W2895035716 modified "2023-10-12" @default.
- W2895035716 title "Smart pH responsive drug delivery system based on poly(HEMA-co-DMAEMA) nanohydrogel" @default.
- W2895035716 cites W1778592536 @default.
- W2895035716 cites W1831107102 @default.
- W2895035716 cites W1967582830 @default.
- W2895035716 cites W1970345694 @default.
- W2895035716 cites W1979975654 @default.
- W2895035716 cites W1983989454 @default.
- W2895035716 cites W1984874612 @default.
- W2895035716 cites W1990218610 @default.
- W2895035716 cites W1996697333 @default.
- W2895035716 cites W2015006203 @default.
- W2895035716 cites W2016156919 @default.
- W2895035716 cites W2019481323 @default.
- W2895035716 cites W2025554542 @default.
- W2895035716 cites W2028705917 @default.
- W2895035716 cites W2029655376 @default.
- W2895035716 cites W2029987677 @default.
- W2895035716 cites W2030085511 @default.
- W2895035716 cites W2031806297 @default.
- W2895035716 cites W2032961593 @default.
- W2895035716 cites W2040549484 @default.
- W2895035716 cites W2041322047 @default.
- W2895035716 cites W2041814283 @default.
- W2895035716 cites W2042617428 @default.
- W2895035716 cites W2044656113 @default.
- W2895035716 cites W2045872960 @default.
- W2895035716 cites W2046425506 @default.
- W2895035716 cites W2046799161 @default.
- W2895035716 cites W2048829256 @default.
- W2895035716 cites W2050576976 @default.
- W2895035716 cites W2053237892 @default.
- W2895035716 cites W2054745605 @default.
- W2895035716 cites W2056993712 @default.
- W2895035716 cites W2060256402 @default.
- W2895035716 cites W2067310377 @default.
- W2895035716 cites W2072997205 @default.
- W2895035716 cites W2075028063 @default.
- W2895035716 cites W2079960550 @default.
- W2895035716 cites W2081938664 @default.
- W2895035716 cites W2086269064 @default.
- W2895035716 cites W2089773350 @default.
- W2895035716 cites W2094449638 @default.
- W2895035716 cites W2096675036 @default.
- W2895035716 cites W2103818266 @default.
- W2895035716 cites W2113287687 @default.
- W2895035716 cites W2118509324 @default.
- W2895035716 cites W2123987464 @default.
- W2895035716 cites W2126991353 @default.
- W2895035716 cites W2145091626 @default.
- W2895035716 cites W2148428528 @default.
- W2895035716 cites W2154149687 @default.
- W2895035716 cites W2156344316 @default.
- W2895035716 cites W2170808477 @default.
- W2895035716 cites W2181113888 @default.
- W2895035716 cites W2207973369 @default.
- W2895035716 cites W2237967761 @default.
- W2895035716 cites W2284013896 @default.
- W2895035716 cites W2287161843 @default.
- W2895035716 cites W2298659816 @default.
- W2895035716 cites W2373434483 @default.
- W2895035716 cites W2404933325 @default.
- W2895035716 cites W2410522720 @default.
- W2895035716 cites W2411145445 @default.
- W2895035716 cites W2522541109 @default.
- W2895035716 cites W2537306461 @default.
- W2895035716 cites W2558700033 @default.
- W2895035716 cites W2569683706 @default.
- W2895035716 cites W2576704366 @default.
- W2895035716 cites W2588888588 @default.
- W2895035716 cites W2597635107 @default.
- W2895035716 cites W2599221812 @default.
- W2895035716 cites W2606251873 @default.
- W2895035716 cites W2607472915 @default.
- W2895035716 cites W2607643319 @default.
- W2895035716 cites W2616129231 @default.
- W2895035716 cites W2627162351 @default.
- W2895035716 cites W2793765713 @default.
- W2895035716 cites W2799706469 @default.
- W2895035716 doi "https://doi.org/10.1016/j.ijpharm.2018.10.001" @default.
- W2895035716 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30291961" @default.
- W2895035716 hasPublicationYear "2018" @default.
- W2895035716 type Work @default.
- W2895035716 sameAs 2895035716 @default.
- W2895035716 citedByCount "69" @default.
- W2895035716 countsByYear W28950357162019 @default.
- W2895035716 countsByYear W28950357162020 @default.
- W2895035716 countsByYear W28950357162021 @default.
- W2895035716 countsByYear W28950357162022 @default.
- W2895035716 countsByYear W28950357162023 @default.
- W2895035716 crossrefType "journal-article" @default.