2015
DOI: 10.1016/j.ejpb.2015.07.005
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The chemotherapeutic potential of doxorubicin-loaded PEG-b-PLGA nanopolymersomes in mouse breast cancer model

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Cited by 82 publications
(31 citation statements)
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“…[35] However, ac omparison of the IC 50 value of the DOX-loaded BAB 3 micelles with other potentiald rug carriers ystems, such as nanopolymersomes, shows af our-fold higher cytotoxicity for DOX-loaded BAB 3 micelles combinedw ith superior biocompatibility. [1] Hence, the DOX-loaded micelles showg ood apoptosis inductiona ctivity in HeLa cells. Consequently the designed BAB 3 micelles are potent candidates for an ovel pH-controlled drugdelivery system with sustained releaseproperties.…”
Section: Intracellular Dox Release and Antitumor Activitymentioning
confidence: 97%
See 1 more Smart Citation
“…[35] However, ac omparison of the IC 50 value of the DOX-loaded BAB 3 micelles with other potentiald rug carriers ystems, such as nanopolymersomes, shows af our-fold higher cytotoxicity for DOX-loaded BAB 3 micelles combinedw ith superior biocompatibility. [1] Hence, the DOX-loaded micelles showg ood apoptosis inductiona ctivity in HeLa cells. Consequently the designed BAB 3 micelles are potent candidates for an ovel pH-controlled drugdelivery system with sustained releaseproperties.…”
Section: Intracellular Dox Release and Antitumor Activitymentioning
confidence: 97%
“…The treatment of canceri sg enerally attempted by surgical removal of the affected tissuei nc ombination with radiation and chemotherapy.T reatment with chemotherapeutic agents, in particular, is often accompanied by undesirable severe side effects, such as the developmento f drug resistance and severe cardiact oxicity,a so bserved for doxorubicin (DOX) baseda nticancer treatments. [1] In general, these systemically administered therapeutic agents suffer from numerousi ssues, for example, hydrophobicity,i nefficient distribution, systemict oxicity,a nd low targeting capability.I nt urn, this decreases the efficiencyo ft hese treatments and puts extra strain on the patient by also affectingh ealthy tissue. [2] Fundamental problems associated with drug administration, including poor selectivity between malignant and innoxious cells, difficulties in adjusting drug dosages, andvarious biological hurdles,c an be addressed by nanomedicine.…”
Section: Introductionmentioning
confidence: 99%
“…(a), approximately 25% of PeaT1 protein can be released from P@NPs within the first 24 h in PBS medium, which were followed by continuous slow release behaviors in the following 7 days. The rapid release in the first several hours was related to protein absorbed/encapsulated on or near the nanoparticle surfaces . The sustained release indicated that release was dependent on diffusion and/or matrix erosion …”
Section: Resultsmentioning
confidence: 99%
“…The rapid release in the first several hours was related to protein absorbed/encapsulated on or near the nanoparticle surfaces. 25 The sustained release indicated that release was dependent on diffusion and/or matrix erosion. 26…”
Section: In Vitro Release Of P@npsmentioning
confidence: 99%
“…The results for the free DOX group could be related to the previously reported toxicities that cause weight loss in mice, such as cardiotoxicity, neurotoxicity and nephrotoxicity. [45][46][47] Unlike the control and free DOX groups, the enhanced anticancer effects and reduced toxicities from application of the nGO@DOX-cPEG flakes (Supplementary Figure S8) led to accumulation and efficient delivery of DOX to tumor sites, which may be due to the sustained release and prolonged circulation in the bloodstream and the enhanced permeation and retention effect. 47,48 In addition, histopathological and immunohistochemical analyses were performed on the tumor masses to determine the expression levels of caspase-3, PARP, CD31 and Ki-67 (Figure 7c; Supplementary Table S2).…”
Section: Resultsmentioning
confidence: 99%