Regional Intestinal Drug Absorption

The gastrointestinal tract (GIT) can be broadly divided into several regions: the stomach, the small intestine (which is subdivided to duodenum, jejunum, and ileum), and the colon. The conditions and environment in each of these segments, and even within the segment, are dependent on many factors, e...

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description The gastrointestinal tract (GIT) can be broadly divided into several regions: the stomach, the small intestine (which is subdivided to duodenum, jejunum, and ileum), and the colon. The conditions and environment in each of these segments, and even within the segment, are dependent on many factors, e.g., the surrounding pH, fluid composition, transporters expression, metabolic enzymes activity, tight junction resistance, different morphology along the GIT, variable intestinal mucosal cell differentiation, changes in drug concentration (in cases of carrier-mediated transport), thickness and types of mucus, and resident microflora. Each of these variables, alone or in combination with others, can fundamentally alter the solubility/dissolution, the intestinal permeability, and the overall absorption of various drugs. This is the underlying mechanistic basis of regional-dependent intestinal drug absorption, which has led to many attempts to deliver drugs to specific regions throughout the GIT, aiming to optimize drug absorption, bioavailability, pharmacokinetics, and/or pharmacodynamics. In the book "Regional Intestinal Drug Absorption: Biopharmaceutics and Drug Formulation" we aim to highlight the current progress and to provide an overview of the latest developments in the field of regional-dependent intestinal drug absorption and delivery, as well as pointing out the unmet needs of the field.
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publisher MDPI - Multidisciplinary Digital Publishing Institute
publisherStr MDPI - Multidisciplinary Digital Publishing Institute
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spelling doab-20.500.12854ir-810512024-03-31T13:10:24Z Regional Intestinal Drug Absorption Gonzalez-Alvarez, Maria Isabel Dahan, Arik bioequivalence Biopharmaceutics Classification System in vitro dissolution test pravastatin oral absorption in silico modeling GastroPlus Phoenix WinNonlin pharmacokinetics clinical studies ibuprofen manometry gastrointestinal mechanistic modeling PBPK PBBM disintegration dissolution enteric-coated ICH quality control regional intestinal permeability permeation enhancers absorption-modifying excipients oral peptide delivery intestinal perfusion pharmaceutical development controlled release drug product biopharmaceutics classification system drug solubility drug permeability location-dependent absorption segregated flow intestinal model (SFM) traditional model (TM) route-dependent intestinal metabolism first-pass effect drug-drug interactions DDI in vitro in vivo extrapolations IVIVE zero-order absorption first-order absorption combined zero- and first-order absorption transit compartment absorption model in situ perfusion microdevices shape mucoadhesion colon absorption nutrient digestion nutrient absorption gastrointestinal hormone postprandial glycaemia energy intake region of the gut obesity type 2 diabetes Franz–PAMPA BCS drugs biomimetic membrane Franz cell passive drug transport BCS class IV drugs segmental-dependent intestinal permeability intestinal absorption oral drug delivery biopharmaceutics physiologically-based pharmacokinetic (PBPK) modeling furosemide intestinal permeability human colon carcinoma cell layer (Caco-2) hierarchical support vector regression (HSVR) drug absorption drug solubility/dissolution regional/segmental-dependent permeability and absorption thema EDItEUR::M Medicine and Nursing thema EDItEUR::K Economics, Finance, Business and Management::KN Industry and industrial studies::KND Manufacturing industries The gastrointestinal tract (GIT) can be broadly divided into several regions: the stomach, the small intestine (which is subdivided to duodenum, jejunum, and ileum), and the colon. The conditions and environment in each of these segments, and even within the segment, are dependent on many factors, e.g., the surrounding pH, fluid composition, transporters expression, metabolic enzymes activity, tight junction resistance, different morphology along the GIT, variable intestinal mucosal cell differentiation, changes in drug concentration (in cases of carrier-mediated transport), thickness and types of mucus, and resident microflora. Each of these variables, alone or in combination with others, can fundamentally alter the solubility/dissolution, the intestinal permeability, and the overall absorption of various drugs. This is the underlying mechanistic basis of regional-dependent intestinal drug absorption, which has led to many attempts to deliver drugs to specific regions throughout the GIT, aiming to optimize drug absorption, bioavailability, pharmacokinetics, and/or pharmacodynamics. In the book "Regional Intestinal Drug Absorption: Biopharmaceutics and Drug Formulation" we aim to highlight the current progress and to provide an overview of the latest developments in the field of regional-dependent intestinal drug absorption and delivery, as well as pointing out the unmet needs of the field. 2022-05-06T11:24:37Z 2022-05-06T11:24:37Z 2022 book ONIX_20220506_9783036536583_117 9783036536583 9783036536576 https://directory.doabooks.org/handle/20.500.12854/81051 eng image/jpeg Attribution 4.0 International https://mdpi.com/books/pdfview/book/5393 https://mdpi.com/books/pdfview/book/5393 MDPI - Multidisciplinary Digital Publishing Institute 10.3390/books978-3-0365-3657-6 10.3390/books978-3-0365-3657-6 46cabcaa-dd94-4bfe-87b4-55023c1b36d0 9783036536583 9783036536576 238 Basel open access
spellingShingle bioequivalence
Biopharmaceutics Classification System
in vitro
dissolution test
pravastatin
oral absorption
in silico modeling
GastroPlus
Phoenix WinNonlin
pharmacokinetics
clinical studies
ibuprofen
manometry
gastrointestinal
mechanistic modeling
PBPK
PBBM
disintegration
dissolution
enteric-coated
ICH
quality control
regional intestinal permeability
permeation enhancers
absorption-modifying excipients
oral peptide delivery
intestinal perfusion
pharmaceutical development
controlled release drug product
biopharmaceutics classification system
drug solubility
drug permeability
location-dependent absorption
segregated flow intestinal model (SFM)
traditional model (TM)
route-dependent intestinal metabolism
first-pass effect
drug-drug interactions
DDI
in vitro in vivo extrapolations
IVIVE
zero-order absorption
first-order absorption
combined zero- and first-order absorption
transit compartment absorption model
in situ perfusion
microdevices
shape
mucoadhesion
colon absorption
nutrient digestion
nutrient absorption
gastrointestinal hormone
postprandial glycaemia
energy intake
region of the gut
obesity
type 2 diabetes
Franz–PAMPA
BCS drugs
biomimetic membrane
Franz cell
passive drug transport
BCS class IV drugs
segmental-dependent intestinal permeability
intestinal absorption
oral drug delivery
biopharmaceutics
physiologically-based pharmacokinetic (PBPK) modeling
furosemide
intestinal permeability
human colon carcinoma cell layer (Caco-2)
hierarchical support vector regression (HSVR)
drug absorption
drug solubility/dissolution
regional/segmental-dependent permeability and absorption
thema EDItEUR::M Medicine and Nursing
thema EDItEUR::K Economics, Finance, Business and Management::KN Industry and industrial studies::KND Manufacturing industries
Regional Intestinal Drug Absorption
title Regional Intestinal Drug Absorption
title_full Regional Intestinal Drug Absorption
title_fullStr Regional Intestinal Drug Absorption
title_full_unstemmed Regional Intestinal Drug Absorption
title_short Regional Intestinal Drug Absorption
title_sort regional intestinal drug absorption
topic bioequivalence
Biopharmaceutics Classification System
in vitro
dissolution test
pravastatin
oral absorption
in silico modeling
GastroPlus
Phoenix WinNonlin
pharmacokinetics
clinical studies
ibuprofen
manometry
gastrointestinal
mechanistic modeling
PBPK
PBBM
disintegration
dissolution
enteric-coated
ICH
quality control
regional intestinal permeability
permeation enhancers
absorption-modifying excipients
oral peptide delivery
intestinal perfusion
pharmaceutical development
controlled release drug product
biopharmaceutics classification system
drug solubility
drug permeability
location-dependent absorption
segregated flow intestinal model (SFM)
traditional model (TM)
route-dependent intestinal metabolism
first-pass effect
drug-drug interactions
DDI
in vitro in vivo extrapolations
IVIVE
zero-order absorption
first-order absorption
combined zero- and first-order absorption
transit compartment absorption model
in situ perfusion
microdevices
shape
mucoadhesion
colon absorption
nutrient digestion
nutrient absorption
gastrointestinal hormone
postprandial glycaemia
energy intake
region of the gut
obesity
type 2 diabetes
Franz–PAMPA
BCS drugs
biomimetic membrane
Franz cell
passive drug transport
BCS class IV drugs
segmental-dependent intestinal permeability
intestinal absorption
oral drug delivery
biopharmaceutics
physiologically-based pharmacokinetic (PBPK) modeling
furosemide
intestinal permeability
human colon carcinoma cell layer (Caco-2)
hierarchical support vector regression (HSVR)
drug absorption
drug solubility/dissolution
regional/segmental-dependent permeability and absorption
thema EDItEUR::M Medicine and Nursing
thema EDItEUR::K Economics, Finance, Business and Management::KN Industry and industrial studies::KND Manufacturing industries
topic_facet bioequivalence
Biopharmaceutics Classification System
in vitro
dissolution test
pravastatin
oral absorption
in silico modeling
GastroPlus
Phoenix WinNonlin
pharmacokinetics
clinical studies
ibuprofen
manometry
gastrointestinal
mechanistic modeling
PBPK
PBBM
disintegration
dissolution
enteric-coated
ICH
quality control
regional intestinal permeability
permeation enhancers
absorption-modifying excipients
oral peptide delivery
intestinal perfusion
pharmaceutical development
controlled release drug product
biopharmaceutics classification system
drug solubility
drug permeability
location-dependent absorption
segregated flow intestinal model (SFM)
traditional model (TM)
route-dependent intestinal metabolism
first-pass effect
drug-drug interactions
DDI
in vitro in vivo extrapolations
IVIVE
zero-order absorption
first-order absorption
combined zero- and first-order absorption
transit compartment absorption model
in situ perfusion
microdevices
shape
mucoadhesion
colon absorption
nutrient digestion
nutrient absorption
gastrointestinal hormone
postprandial glycaemia
energy intake
region of the gut
obesity
type 2 diabetes
Franz–PAMPA
BCS drugs
biomimetic membrane
Franz cell
passive drug transport
BCS class IV drugs
segmental-dependent intestinal permeability
intestinal absorption
oral drug delivery
biopharmaceutics
physiologically-based pharmacokinetic (PBPK) modeling
furosemide
intestinal permeability
human colon carcinoma cell layer (Caco-2)
hierarchical support vector regression (HSVR)
drug absorption
drug solubility/dissolution
regional/segmental-dependent permeability and absorption
thema EDItEUR::M Medicine and Nursing
thema EDItEUR::K Economics, Finance, Business and Management::KN Industry and industrial studies::KND Manufacturing industries
url ONIX_20220506_9783036536583_117