2012
DOI: 10.1039/c2ra21087h
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Cytotoxicity and slow release of the anti-cancer drug doxorubicin from ZIF-8

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Cited by 267 publications
(165 citation statements)
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References 49 publications
(81 reference statements)
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“…In this study, the doxorubicin: ZIF-8 complex, which aims to treat mucoepidermoid carcinoma of human lung, human colorectal adenocarcinoma (HT-29) and human promyelocytic leukaemia (HL-60) cell lines, exhibits lower toxicity than pure doxorubicin, probably due to the slow release of the drug that is achieved with this complex (Figure 6) [69,104]. Furthermore, ZIF-8 crystals loaded with doxorubicin proved to be efficient pH-responsive drug delivery systems, in which the drug is released in a controlled manner at low pH (5.0-6.5).…”
Section: Slow Release Of the Anti-cancer Drug Doxorubicin From Zif-8mentioning
confidence: 99%
See 1 more Smart Citation
“…In this study, the doxorubicin: ZIF-8 complex, which aims to treat mucoepidermoid carcinoma of human lung, human colorectal adenocarcinoma (HT-29) and human promyelocytic leukaemia (HL-60) cell lines, exhibits lower toxicity than pure doxorubicin, probably due to the slow release of the drug that is achieved with this complex (Figure 6) [69,104]. Furthermore, ZIF-8 crystals loaded with doxorubicin proved to be efficient pH-responsive drug delivery systems, in which the drug is released in a controlled manner at low pH (5.0-6.5).…”
Section: Slow Release Of the Anti-cancer Drug Doxorubicin From Zif-8mentioning
confidence: 99%
“…ZIFs simultaneously have the following characteristics of MOFs and zeolites, combining the advantages of both: ultrahigh surface areas, unimodal micropores, high crystallinity, various functionalities and exceptional thermal and chemical stabilities, making them very promising for biomedical applications [63,64]. Several studies describe the successful incorporation of anticancer drugs into ZIF-8 with positive results for the controlled pH-sensitive drug release and fluorescence imaging [65][66][67][68][69]. Also caffeine was already encapsulated into ZIF-8 showing a controlled release [70,71].…”
Section: Introductionmentioning
confidence: 99%
“…This increases drug concentration at the target site and is expected to be a more efficient technique than the standard methods of drug delivery. Doxorubicin (DoX) is a low molecular weight, anthracycline drug which is effective against a wide range of malignant conditions, especially lukemia and lymphoma, as well as cancers of bladder, breast, stomach, lung and ovaries [9,10]. However, the drug possesses a cumulative dose-dependent cardiotoxicity and can lead to drug-induced congestive heart failure [10,11].…”
Section: Introductionmentioning
confidence: 99%
“…Doxorubicin (DoX) is a low molecular weight, anthracycline drug which is effective against a wide range of malignant conditions, especially lukemia and lymphoma, as well as cancers of bladder, breast, stomach, lung and ovaries [9,10]. However, the drug possesses a cumulative dose-dependent cardiotoxicity and can lead to drug-induced congestive heart failure [10,11]. Controlling or reducing the dose of DoX is known to prevent the significant risk factors enabling its use for long term chemotherapy [9].…”
Section: Introductionmentioning
confidence: 99%
“…The ZnBDC framework kept the same crystal structure before and after contact with the Gen solution for a time period of up to 7 days ( Figure S4, SI section). 28,57 Conversely, the XRD patterns for ZIF-8 before and after contact with Gen shows alterations ( Figure S5, SI section), which may indicate drug adsorption to the framework (see further discussion of the TGA data below). The XRD patterns of the frameworks present thin peaks, indicating high crystallinity and in good agreement with previous studies reported in the literature.…”
mentioning
confidence: 99%