2017
DOI: 10.1111/jphp.12692
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Preparation, pharmacokinetics and tumour-suppressive activity of berberine liposomes

Abstract: Our study suggested that BBR liposomes may provide a safe form of intravenous drug therapy for strengthening the antitumour effects of BBR.

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Cited by 39 publications
(20 citation statements)
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“…In agreement with the in vitro data, we obtained the first in vivo evidence for the enhanced efficacy of the berberine combined with PEG-lip-DOX in tumor-bearing mice. Although the precise function of berberine for the enhancement of this anticancer effect by the combination with liposomal DOX is not clear at present, liposomalization of berberine 12) would be valuable future work to further enhance the combination effects. During the study, the body weight of all groups was monitored; however, none of the treatments affected the body weight very much (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…In agreement with the in vitro data, we obtained the first in vivo evidence for the enhanced efficacy of the berberine combined with PEG-lip-DOX in tumor-bearing mice. Although the precise function of berberine for the enhancement of this anticancer effect by the combination with liposomal DOX is not clear at present, liposomalization of berberine 12) would be valuable future work to further enhance the combination effects. During the study, the body weight of all groups was monitored; however, none of the treatments affected the body weight very much (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…Thus, liposomes of 100–200 nm in size have been considered as suitable for their distribution in the three infected organs (liver, spleen and BM). Different methods have been previously used for the obtention of common BER liposomes, such as the pH gradient-film method [ 31 ] or ethanol injection method [ 18 ], with variable encapsulation efficacies (85 and 10.4%). In this study, we prepared liposomes by film-hydration method and homogenization of their size by sonication.…”
Section: Discussionmentioning
confidence: 99%
“…The pharmacokinetic characteristics of BER as well as its organ accumulation have been much more widely investigated in rats [ 31 , 54 ]. According to Cl value in rats, BER would present an intermediate rate of clearance [ 31 ], whereas it would be considered as very rapid in mice. Although LP-BER decreased the clearance of the drug by 10-fold, it was still very high.…”
Section: Discussionmentioning
confidence: 99%
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“…To prolong the release and increase the bioavailability of BH, the administration of drug encapsulated in biodegradable polymeric nanoparticles has been investigated. For example, solid lipid nanoparticles (Wang et al, 2017), gold nanoparticles (Yu et al, 2016), and so on. Despite these, the reported nanodosage forms of BH still have low oral bioavailability and many side effects that need to be overcome (Su et al, 2019).…”
Section: Introductionmentioning
confidence: 99%