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Modelagem farmacocinética e análise de sistemas lineares para a predição da concentração de medicamentos no corpo humano.

2012· dissertation· pt· W1909511508 on OpenAlexaff
Milton Gallo Neto

Bibliographic record

Venuenot available
Typedissertation
Languagept
FieldMedicine
TopicPharmaceutical studies and practices
Canadian institutionsCanadian Association of Nurses in Oncology
Fundersnot available
KeywordsTransdermalPharmacokineticsCompartment (ship)PharmacologyDrugChemistryMedicine

Abstract

fetched live from OpenAlex

The pharmacokinetic modeling can predict the concentration of drug in different tissues of the human body.The development of mathematical models is an important tool to verify the appropriateness of certain procedures performed in medication administration.The objective of this work is to develop a pharmacokinetic model able to predict the plasma concentration of drug in the body after various forms of infusion.Two approaches were used.Initially, in the one-compartment approach it was considered that the drug enters the body directly into the blood compartment, which represents the entire human body.In the two-compartment approach it was considered the following compartments: one representing the means by which the drug is infused into the body (either via the gastrointestinal tract, lung, or transdermal) and one representing the blood plasma.In both cases, it was considered homogeneous concentration of the drug in the compartments.The model was built by using block diagrams and the solution was obtained using the Laplace Transform.The model was validated by comparing its results to literature data, with very good agreement.The model allowed comparing the one-compartment constant infusion of drug in the body with the periodic infusion.The analysis of the results generated by the model showed that the concentrations achieved by these methods are not the same.The two-compartment model allowed simulating oral and transdermal administration, and inhalation.It was possible to predict blood concentration after interruption of therapy with anti-depressants and anti-conceptional drugs.The model was able to verify the time it takes to reach the former level.Methods have been proposed to achieve the same concentration in a shorter period of time.Another application was the comparison of the treatment with whole tablets and taken by half in a smaller interval of time.It was found that the concentration achieved is different even though the same mass is ingested in both cases.The model was also used to calculate the concentration of nicotine after cigarette smoking and it was found that the individual who smokes every three hours, nicotine is not entirely eliminated from body.Furthermore, it was possible to simulate overdose of an anti-inflammatory and the period of time when the concentration is above the therapeutic level.It has been proposed a method to obtain pharmacokinetic parameter related to absorption, which can be easily obtained based on data present in the drug bull.This method is much simpler and more accurate than the method proposed in the, which uses graphical analysis and clinical data that are not so easy to be obtained.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.002
metaresearch head score (Gemma)0.008
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Simulation or modeling · Consensus signal: Simulation or modeling
GenreCandidate signal: Empirical · Consensus signal: none
Teacher disagreement score0.024
Threshold uncertainty score0.048

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0020.008
Meta-epidemiology (narrow)0.0010.001
Meta-epidemiology (broad)0.0010.003
Bibliometrics0.0010.001
Science and technology studies0.0010.000
Scholarly communication0.0020.001
Open science0.0010.001
Research integrity0.0020.002
Insufficient payload (model declined to judge)0.0060.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.110
GPT teacher head0.416
Teacher spread0.306 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designSimulation or modeling
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2012
Admission routes1
Has abstractyes

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