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Sökning: L773:0939 6411 OR L773:1873 3441 > (2020-2024) > Pulmonary drug abso...

Pulmonary drug absorption and systemic exposure in human : Predictions using physiologically based biopharmaceutics modeling

Eriksson, Johanna (författare)
Uppsala universitet,Institutionen för farmaci
Thorn, Helena (författare)
AstraZeneca, Inhalat PD Unit, Operat, Pharmaceut Technol & Dev, Gothenburg, Sweden.
Lennernäs, Hans (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
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Sjögren, Erik, 1977- (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
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 (creator_code:org_t)
ELSEVIER, 2020
2020
Engelska.
Ingår i: European journal of pharmaceutics and biopharmaceutics. - : ELSEVIER. - 0939-6411 .- 1873-3441. ; 156, s. 191-202
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Systemic exposure of inhaled drugs is used to estimate the local lung exposure and assess systemic side effects for drugs with local pharmacological targets. Predicting systemic exposure is therefore central for successful development of drugs intended to be inhaled. Currently, these predictions are based mainly on data from in vitro experiments, but the accuracy of these predictions might be improved if they were based on data with higher physiological relevance. In this study, systemic exposure was simulated by applying biopharmaceutics input parameters from isolated perfused rat lung (IPL) data to a lung model developed in MoBi (R) as an extension to the full physiologically-based pharmacokinetic (PBPK) model in PK-Sim (R). These simulations were performed for a set of APIs with a variety of physicochemical properties and formulation types. Simulations based on rat IPL data were also compared to simulations based on in vitro data. The predictive performances of the simulations were evaluated by comparing simulated plasma concentration-time profiles to clinical observations after pulmonary administration. Simulations using IPL-based input parameters predicted systemic exposure well, with predicted AUCs within two-fold of the observed value for nine out of ten drug compounds/formulations, and predicted Cmax values within two-fold for eight out of ten drug compounds/formulations. Simulations using input parameters based on IPL data performed generally better than simulations based on in vitro input parameters. These results suggest that the developed model in combination with IPL data can be used to predict human lung absorption for compounds with different physicochemical properties and types of inhalation formulations.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)

Nyckelord

Prediction of systemic exposure
Pulmonary drug absorption
Physiological based biopharmaceutics modeling
Isolated perfused lung

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