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The influence of the gut microbiota on the bioavailability of oral drugs.
Zhang, Xintong; Han, Ying; Huang, Wei; Jin, Mingji; Gao, Zhonggao.
Afiliación
  • Zhang X; State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Department of Pharmaceutics, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
  • Han Y; State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Department of Pharmaceutics, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
  • Huang W; State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Department of Pharmaceutics, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
  • Jin M; State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Department of Pharmaceutics, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
  • Gao Z; State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Department of Pharmaceutics, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.
Acta Pharm Sin B ; 11(7): 1789-1812, 2021 Jul.
Article en En | MEDLINE | ID: mdl-34386321
Palabras clave
5-ASA, 5-aminosalicylic acid; AA, ascorbic acid; ABC, ATP-binding cassette; ACS, amphipathic chitosan derivative; AMI, amiodarone; AQP4, aquaporin 4; AR, azoreductase; ASP, amisulpride; BBR, berberine; BCRP, breast cancer resistance protein; BCS, biopharmaceutics classification system; BDDCS, the biopharmaceutics drug disposition classification system; BDEPT, the bacteria-directed enzyme prodrug therapy; BSH, bile salt hydrolase; Bioavailability; CA, cholic acid; CDCA, chenodeoxycholic acid; CPP, cell-penetrating peptide; CS, chitosan; Colon-specific drug delivery system; DCA, deoxycholic acid; DRPs, digoxin reduction products; EcN, Escherichia coli Nissle 1917; FA, folate; FAO, Food and Agriculture Organization of the United Nations; GCDC, glycochenodeoxycholate; GL, glycyrrhizic acid; Gut microbiota; HFD, high fat diet; HTC, hematocrit; IBD, inflammatory bowel disease; LCA, lithocholic acid; LPS, lipopolysaccharide; MATEs, multidrug and toxin extrusion proteins; MDR1, multidrug resistance gene 1; MDR1a, multidrug resistance protein-1a; MKC, monoketocholic acid; MPA, mycophenolic acid; MRP2, multidrug resistance-associated protein 2; NEC, necrotizing enterocolitis; NMEs, new molecular entities; NRs, nitroreductases; NSAIDs, non-steroidal anti-inflammatory drugs; NaDC, sodium deoxycholate; NaGC, sodium glycholate; OATs, organic anion transporters; OCTNs, organic zwitterion/cation; OCTs, organic cation transporters; Oral drugs; P-gp, P-glycoprotein; PD, Parkinson's disease; PPIs, proton pump inhibitors; PT, pectin; PWSDs, poorly water-soluble drugs; Probiotics; RA, rheumatoid arthritis; RBC, red blood cell; SCFAs, short-chain fatty acids; SGLT-1, sodium-coupled glucose transporter 1; SLC, solute carrier; SLN, solid lipid nanoparticle; SP, sulfapyridine; SSZ, sulfasalazine; SVCT-1/2, the sodium-dependent vitamin C transporter-1/2; T1D, type 1 diabetes; T1DM, type 1 diabetes mellitus; T2D, type 2 diabetes; TCA, taurocholate; TCDC, taurochenodeoxycholate; TDCA, taurodeoxycholate; TLCA, taurolithocholate; TME, the tumor microenvironment; UDC, ursodeoxycholic acid; WHO, World Health Organization; an OTC drug, an over-the-counter drug; cgr operon, cardiac glycoside reductase operon; dhBBR, dihydroberberine; pKa, dissociation constant; the GI tract, the gastrointestinal tract

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Acta Pharm Sin B Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Acta Pharm Sin B Año: 2021 Tipo del documento: Article