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Record W2763937928

Investigation of Amorphous Solid Dispersions of Poorly Water-soluble Drugs in Poly (2-hydroxyethyl Methacrylate) Hydrogels for Enhanced Solubility and Controlled Release

2014· dissertation· en· W2763937928 on OpenAlexfundno aff
Dajun Sun

Bibliographic record

VenueTSpace (University of Toronto) · 2014
Typedissertation
Languageen
FieldPharmacology, Toxicology and Pharmaceutics
TopicDrug Solubulity and Delivery Systems
Canadian institutionsnot available
FundersNatural Sciences and Engineering Research Council of CanadaUniversity of Toronto
Keywords2-Hydroxyethyl MethacrylateSelf-healing hydrogelsSolubilityMethacrylateAmorphous solidMaterials scienceChemical engineeringPolymer chemistry(Hydroxyethyl)methacrylateChemistryPolymerOrganic chemistryComposite materialCopolymer
DOInot available

Abstract

fetched live from OpenAlex

The purpose of this study was to investigate the potential of applying amorphous solid dispersions (ASD) in crosslinked PHEMA hydrogels to enhance the dissolution behavior of poorly water-soluble drugs. The first part of the study identifies physicochemical properties affecting the solid state and physical stability of ASD of the model drug indomethacin (IND) in PHEMA hydrogels. The results of the second part show that ASD based on water-insoluble crosslinked PHEMA can maintain a high level of supersaturation over a prolonged duration via a diffusion-controlled feedback mechanism, thus avoiding the initial surge of supersaturation followed by a sharp decline in drug concentration, which is typically encountered with ASD based on water-soluble polymers (e.g., PVP, HPMCAS) under nonsink dissolution conditions. A subsequent study examines the effect of supersaturation generation rate on the resulting kinetic solubility profiles of amorphous pharmaceuticals and delineates the interplay between dissolution and precipitation processes from a mechanistic viewpoint. In the absence of any dissolved polymer to inhibit drug precipitation from the supersaturated state, both our experimental and predicted results confirm that the faster rise of the kinetic solubility profile of an amorphous drug will inevitably lead to an earlier but higher maximum kinetic solubility and a sharper decline in the de-supersaturation phase, and vice versa. The relationship between the achievable maximum supersaturation and the rate of supersaturation generation in the observed kinetic solubility profiles has been described for the first time by our comprehensive mechanistic model taking into account the role of supersaturation in both the nucleation and crystallization processes as well as the associated competitive particle growth and ripening effects. Finally, this theoretical framework was further employed to semi-quantitatively predict the evolution of supersaturation of amorphous pharmaceuticals generated from nonlinear dissolution profiles. The effects of initial degree of supersaturation, dissolution of amorphous drug and that from the IND-PHEMA ASD under nonsink dissolution conditions were subsequently examined in detail. The comparison of dissolution behaviors between amorphous IND and IND-PHEMA ASD demonstrates the advantage of the diffusion-controlled feedback mechanism that makes crosslinked PHEMA a unique and desirable carrier for amorphous drug delivery systems.

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 distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow), Insufficient payload (model declined to judge)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.101
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0010.000
Insufficient payload (model declined to judge)0.0010.000

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 head0.035
GPT teacher head0.337
Teacher spread0.303 · 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 teacher head, not a consensus.

Study designBench or experimental
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".

Quick stats

Citations0
Published2014
Admission routes1
Has abstractyes

Explore more

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