نتایج جستجو برای: drug transporters

تعداد نتایج: 607253  

Journal: :Pharmacological reviews 2001
G Lee S Dallas M Hong R Bendayan

Drug transport in the central nervous system is highly regulated not only by the blood-brain and the blood-cerebrospinal fluid barriers but also in brain parenchyma. The novel localization of drug transporters in brain parenchyma cells, such as microglia and astrocytes, suggest a reconsideration of the present conceptualization of brain barriers as it relates to drug transport. That is, the cel...

2017
Colby S. Shemesh Rosie Z. Yu Mark S. Warren Michael Liu Mirza Jahic Brandon Nichols Noah Post Song Lin Daniel A. Norris Eunju Hurh Jane Huang Tanya Watanabe Scott P. Henry Yanfeng Wang

Antisense oligonucleotides are metabolized by nucleases and drug interactions with small drug molecules at either the cytochrome P450 (CYP) enzyme or transporter levels have not been observed to date. Herein, a comprehensive in vitro assessment of the drug-drug interaction (DDI) potential was carried out with four 2'-O-(2-methoxyethyl)-modified antisense oligonucleotides (2'-MOE-ASOs), includin...

Journal: :Journal of thee Medical Sciences (Berkala Ilmu Kedokteran) 2015

2018
Longfa Kou Yangzom D. Bhutia Qing Yao Zhonggui He Jin Sun Vadivel Ganapathy

Targeted nano-drug delivery systems conjugated with specific ligands to target selective cell-surface receptors or transporters could enhance the efficacy of drug delivery and therapy. Transporters are expressed differentially on the cell-surface of different cell types, and also specific transporters are expressed at higher than normal levels in selective cell types under pathological conditio...

Journal: :Diabetes 2008
Iouri Bachmakov Hartmut Glaeser Martin F Fromm Jörg König

OBJECTIVE The uptake of drugs into hepatocytes is a key determinant for hepatic metabolism, intrahepatic action, their subsequent systemic plasma concentrations, and extrahepatic actions. In vitro and in vivo studies indicate that many drugs used for treatment of cardiovascular diseases (e.g., oral antidiabetic drugs, statins) are taken up into hepatocytes by distinct organic anion transporters...

Journal: :Journal of tuberculosis research 2022

Introduction: Polymorphisms are the main genetic factors associated with toxicities of antituberculosis drugs. This literature review summarizes polymorphisms genes that code for enzymes metabolism drugs and their transmembrane transporters. Some mechanisms drug-associated strategies management have also been described in this review. Methods: The bibliographic searches were exclusively carried...

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