2008
DOI: 10.1016/j.ctrv.2008.04.003
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Multi-functional nanocarriers to overcome tumor drug resistance

Abstract: The development of resistance to variety of chemotherapeutic agents is one of the major challenges in effective cancer treatment. Tumor cells are able to generate a multi-drug resistance (MDR) phenotype due to microenvironmental selection pressures. This review addresses the use of nanotechnology-based delivery systems to overcome MDR in solid tumors. Our own work along with evidence from the literature illustrates the development of various types of engineered nanocarriers specifically designed to enhance tum… Show more

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Cited by 379 publications
(259 citation statements)
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References 76 publications
(170 reference statements)
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“…1,2 However, these drug carriers are often associated with drawbacks including undesirable burst drug release and premature drug leaking due to their limited stability. Very recently, graphene materials were shown to be capable of loading aromatic anticancer drugs such as doxorubicin (DOX) and camptothecin (CPT) with ultrahigh efficiency.…”
Section: ■ Introductionmentioning
confidence: 99%
“…1,2 However, these drug carriers are often associated with drawbacks including undesirable burst drug release and premature drug leaking due to their limited stability. Very recently, graphene materials were shown to be capable of loading aromatic anticancer drugs such as doxorubicin (DOX) and camptothecin (CPT) with ultrahigh efficiency.…”
Section: ■ Introductionmentioning
confidence: 99%
“…Деякі з цих проблем можуть бути подолані шляхом роз-робки адекватних систем доставки лікарських засобів [4]. Такі системи можуть забезпечити вплив на пухлини протягом тривалого періоду часу внаслідок їх специфічної взаємодії з мембраною злоякісних клітин, не пошко-джуючи при цьому умовно нормальні клітини [5]. Через високу токсичність протипухлин-них препаратів дуже важливим є пошук спо-лук, які б могли зменшувати побічні ефекти хіміотерапії.…”
unclassified
“…The uncertainties led to unsuccessful application of the inhibitors or siRNA on clinical therapies. In fact, therapies that target one MDR pathway were found to enhance the ability of cancer cells to adapt and develop other drug resistance pathways such as alternating efflux transporters 2, 3, 4, 5, 6, 7…”
Section: Introductionmentioning
confidence: 99%