2012
DOI: 10.1016/j.carbpol.2012.04.050
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O-Carboxymethyl chitosan nanoparticles for metformin delivery to pancreatic cancer cells

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Cited by 106 publications
(42 citation statements)
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“…Nanoparticles were taken up nonspecifically by normal and pancreatic cancer cells. Degree of hemolysis caused by drug loaded and blank nanoparticles was less than 5% (Snima et al, 2012). Snima et al (2014) also evaluated the O-carboxymethyl chitosan nanoparticles for pancreatic cancer therapy by means of in vitro (migration assay, clonogenic assay, cell cycle analysis and qRT-PCR analysis) and in vivo (biodistribution studies) studies.…”
Section: Metformin-loaded Microparticles and Nanoparticlesmentioning
confidence: 99%
“…Nanoparticles were taken up nonspecifically by normal and pancreatic cancer cells. Degree of hemolysis caused by drug loaded and blank nanoparticles was less than 5% (Snima et al, 2012). Snima et al (2014) also evaluated the O-carboxymethyl chitosan nanoparticles for pancreatic cancer therapy by means of in vitro (migration assay, clonogenic assay, cell cycle analysis and qRT-PCR analysis) and in vivo (biodistribution studies) studies.…”
Section: Metformin-loaded Microparticles and Nanoparticlesmentioning
confidence: 99%
“…To fulfill this purpose, carboxymethyl chitosan (CM-chitosan), water-soluble derivatives of chitosan with carboxymethyl group was selected due to its controllable self-aggregation and bioadhesive promoting property (Mourya, Inamdar, & Tiwari, 2010;Thanou, Verhoef, & Junginger, 2001). Several studies have utilized CMchitosan to produce nanoparticles through ionic gelation induced by calcium ions (Luo et al, 2013;Shi, Du, Yang, Zhang, & Sun, 2006;Snima, Jayakumar, Unnikrishnan, Nair, & Lakshmanan, 2012). Here it is noted that CM-chitosan with 87e90% DS (degree of substitution) has polyampholytic (zwitter ionic) character, which allows the formation of clear gels or solutions at neutral and alkaline pH values but aggregates under acidic conditions (Thanou et al, 2001).…”
Section: Introductionmentioning
confidence: 99%
“…Туморогенность -только РСК способны иницииро-вать малигнизацию, поэтому их называют «клетки-инициации опухолевого роста», с тем чтобы подчер-кнуть их онкогенный потенциал. Следует отметить еще одну важную черту -РСК яв-ляются гораздо более химио-и радиорезистентными, чем дифференцированные клетки, которые образуют опу-холевую массу, и, таким образом, они ответственны за ле-карственную устойчивость и рецидив опухоли [19,20].…”
Section: влияние на раковые стволовые клеткиunclassified
“…Так, авторы предлагают коинкапсулировать в липосомах метформин и эпирубицин [22]. В последние два года по-явилось множество публикаций, в которых обсуждаются способы доставки метформина [17,19].…”
Section: влияние на раковые стволовые клеткиunclassified