2023
DOI: 10.1016/j.ijbiomac.2023.124370
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Metal-organic framework decorated with glycyrrhetinic acid conjugated chitosan as a pH-responsive nanocarrier for targeted drug delivery

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Cited by 35 publications
(11 citation statements)
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“…In this system, glycyrrhetinic acid-modified chitosan served as a carrier for the chemotherapy drug doxorubicin and was loaded into a metal–organic framework. The liver-targeting ligand glycyrrhetinic acid specifically bound to glycyrrhetinic acid receptors overexpressed on liver cancer cell membrane, providing an active targeting effect for the delivery system [ 167 ].…”
Section: Discussionmentioning
confidence: 99%
“…In this system, glycyrrhetinic acid-modified chitosan served as a carrier for the chemotherapy drug doxorubicin and was loaded into a metal–organic framework. The liver-targeting ligand glycyrrhetinic acid specifically bound to glycyrrhetinic acid receptors overexpressed on liver cancer cell membrane, providing an active targeting effect for the delivery system [ 167 ].…”
Section: Discussionmentioning
confidence: 99%
“…To control these problems, the conjugation of chitosan and PVP has been recommended to enhance the solubility of chitosan at a high pH level [ 238 , 242 ]. Another method was used to successfully fabricate iron (III) carboxylate metal–organic framework NPs coated with a glycyrrhetinic acid–chitosan conjugate (MIL-101/GA-CS), which behaved as a pH-responsive and target-specific agent to deliver DOX for hepatocellular carcinoma (HCC) therapy ( Figure 7 ) [ 243 ]. These NPs have the advantages of a uniform size, drug encapsulation effectiveness, and pH-dependent targeted drug release.…”
Section: Stimuli-sensitive Deliveries Of Chitosan–dox Npsmentioning
confidence: 99%
“…So far, GA as an effective liver-specific targeting molecule has been usually used to decorate liposomes, nanomaterials, micelles, and so on to prepare HCC-targeted drug delivery systems. 42−49 For example, Singh and coworkers reported that GA (as an efficient targeting ligand for HCC) conjugation to epirubicin (as an anticancer drug) significantly enhances targeting ability against HCC both in vitro and in vivo; 45 Cai and coworkers reported that metal−organic framework nanoparticles decorated with GA-conjugated chitosan as pH-responsive and targeted selective systems for doxorubicin delivery demonstrated excellent penetration and cancer-killing capabilities in HCC therapy; 46 Yang and coworkers also demonstrated that the NHC−Au(I) complex containing GA (as an active targeting ligand for HCC) displayed better tumor targeting and anticancer activity toward HCC in vitro and in vivo than that of oxaliplatin. 49 Therefore, the above research results suggested that GA, as a highly efficient targeting ligand, has excellent advantages in drug delivery systems for mediating HCC therapy.…”
Section: ■ Introductionmentioning
confidence: 99%
“…Glycyrrhetinic acid (GA), as a pentacyclic triterpenoid derivative extracted from the herb licorice, which has been often used for hepatocyte-targeting ligand due to its specific receptors on the liver cell membrane, exhibited moderate anticancer activity against liver cancer with diverse antitumor mechanisms. More importantly, many studies suggested that GA could specifically bind to the GA receptor, which is overexpressed on HCC cell lines than that of the adjacent normal liver cells and non-HCC cell lines. Therefore, GA has been widely used as a ligand for liver targeting. So far, GA as an effective liver-specific targeting molecule has been usually used to decorate liposomes, nanomaterials, micelles, and so on to prepare HCC-targeted drug delivery systems. For example, Singh and coworkers reported that GA (as an efficient targeting ligand for HCC) conjugation to epirubicin (as an anticancer drug) significantly enhances targeting ability against HCC both in vitro and in vivo; Cai and coworkers reported that metal–organic framework nanoparticles decorated with GA-conjugated chitosan as pH-responsive and targeted selective systems for doxorubicin delivery demonstrated excellent penetration and cancer-killing capabilities in HCC therapy; Yang and coworkers also demonstrated that the NHC–Au(I) complex containing GA (as an active targeting ligand for HCC) displayed better tumor targeting and anticancer activity toward HCC in vitro and in vivo than that of oxaliplatin . Therefore, the above research results suggested that GA, as a highly efficient targeting ligand, has excellent advantages in drug delivery systems for mediating HCC therapy.…”
Section: Introductionmentioning
confidence: 99%