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Article: Pharmacokinetic Advantage of ASD Device Promote Drug Absorption through the Epicardium

TitlePharmacokinetic Advantage of ASD Device Promote Drug Absorption through the Epicardium
Authors
Keywordsviscosity
Local targeted drug delivery system
cardiac support device
liposolubility
ASD device
Issue Date2020
Citation
Pharmaceutical Research, 2020, v. 37, n. 9, article no. 173 How to Cite?
Abstract© 2020, Springer Science+Business Media, LLC, part of Springer Nature. Purpose: Due to low therapeutic efficacy and severe adverse reaction of systemic administration for coronary heart disease (CHD) therapy, we designed a novel local target delivery system, called Active hydraulic ventricular Support Drug delivery system (ASD). This study aims to investigate the potential advantages of ASD compared to intrapericardial (IPC) injection and factors affecting drug absorption through epicardium. Methods: Liposoluble, water soluble and viscous solutions of cyanine 5 (Cy5) fluorescent dye were delivered individually through ASD and IPC in Sprague-Dawley (SD) rats and then tissues were isolated and observed by in vivo imaging system. Atria and ventricles of the heart were taken for the paraffin section and observed under a fluorescence microscope. Results: The fluorescence intensity of Cy5 injected by ASD distributed in the heart was significantly higher than IPC injection. Whereas, the fluorescence signal spread in other tissues such as lung, liver, spleen, and kidney of ASD groups was much weaker. Moreover, when choosing liposoluble and viscous Cy5, the intensity of the heart turned stronger and fluorescence dye distributed in other tissues was lesser. Conclusions: The application of ASD device may provide a promising route of drug delivery for CHD. Furthermore, increasing viscosity of the solution and liposolublity of the drug was beneficial to facilitate drug absorption through the epicardium.
Persistent Identifierhttp://hdl.handle.net/10722/293140
ISSN
2023 Impact Factor: 3.5
2023 SCImago Journal Rankings: 0.707
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorMikrani, Reyaj-
dc.contributor.authorLi, Cunyu-
dc.contributor.authorNaveed, Muhammad-
dc.contributor.authorLi, Cuican-
dc.contributor.authorBaig, Mirza Muhammad Faran Ashraf-
dc.contributor.authorZhang, Qin-
dc.contributor.authorWang, Yue-
dc.contributor.authorPeng, Juanjuan-
dc.contributor.authorZhao, Lingzhi-
dc.contributor.authorZhou, Xiaohui-
dc.date.accessioned2020-11-19T09:02:04Z-
dc.date.available2020-11-19T09:02:04Z-
dc.date.issued2020-
dc.identifier.citationPharmaceutical Research, 2020, v. 37, n. 9, article no. 173-
dc.identifier.issn0724-8741-
dc.identifier.urihttp://hdl.handle.net/10722/293140-
dc.description.abstract© 2020, Springer Science+Business Media, LLC, part of Springer Nature. Purpose: Due to low therapeutic efficacy and severe adverse reaction of systemic administration for coronary heart disease (CHD) therapy, we designed a novel local target delivery system, called Active hydraulic ventricular Support Drug delivery system (ASD). This study aims to investigate the potential advantages of ASD compared to intrapericardial (IPC) injection and factors affecting drug absorption through epicardium. Methods: Liposoluble, water soluble and viscous solutions of cyanine 5 (Cy5) fluorescent dye were delivered individually through ASD and IPC in Sprague-Dawley (SD) rats and then tissues were isolated and observed by in vivo imaging system. Atria and ventricles of the heart were taken for the paraffin section and observed under a fluorescence microscope. Results: The fluorescence intensity of Cy5 injected by ASD distributed in the heart was significantly higher than IPC injection. Whereas, the fluorescence signal spread in other tissues such as lung, liver, spleen, and kidney of ASD groups was much weaker. Moreover, when choosing liposoluble and viscous Cy5, the intensity of the heart turned stronger and fluorescence dye distributed in other tissues was lesser. Conclusions: The application of ASD device may provide a promising route of drug delivery for CHD. Furthermore, increasing viscosity of the solution and liposolublity of the drug was beneficial to facilitate drug absorption through the epicardium.-
dc.languageeng-
dc.relation.ispartofPharmaceutical Research-
dc.subjectviscosity-
dc.subjectLocal targeted drug delivery system-
dc.subjectcardiac support device-
dc.subjectliposolubility-
dc.subjectASD device-
dc.titlePharmacokinetic Advantage of ASD Device Promote Drug Absorption through the Epicardium-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1007/s11095-020-02898-6-
dc.identifier.pmid32839887-
dc.identifier.scopuseid_2-s2.0-85089747775-
dc.identifier.hkuros320911-
dc.identifier.volume37-
dc.identifier.issue9-
dc.identifier.spagearticle no. 173-
dc.identifier.epagearticle no. 173-
dc.identifier.eissn1573-904X-
dc.identifier.isiWOS:000564930600001-
dc.identifier.issnl0724-8741-

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