Reference health

Controlled Release Matrix Tablets of Olanzapine: Influence of Polymers on the In Vitro Release and Bioavailability

https://doi.org/10.1208/s12249-010-9510-0
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1 of 43 checkable references need attention · checked 2026-07-22

At the dated check, the references listed below either did not resolve in Crossref or DataCite, or carried a retraction notice. Each one is shown with the registry record that put it there.

5 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.

References needing attention

does not resolve to a known work10.1023/A:1015276028425
The 42 checked references that resolve
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Safety and effectiveness of olanzapine in monotherapy: A multivariate analysis of a naturalistic study
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Antipsychotic Medications and Drug‐Induced Movement Disorders Other Than Parkinsonism: A Population‐Based Cohort Study in Older Adults
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Atypical Antipsychotic Drugs and the Risk of Sudden Cardiac Death
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Optimizing Atypical Antipsychotic Treatment Strategies in the Elderly
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Using Drug Claims Data to Assess the Relationship of Medication Adherence With Hospitalization and Costs
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Switching from other antipsychotics to once-daily extended release quetiapine fumarate in patients with schizophrenia
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resolves10.1208/s12249-008-9108-y
Formulation, Release Characteristics and Bioavailability Study of Oral Monolithic Matrix Tablets Containing Carbamazepine
resolves10.1208/pt0804083
Investigations of the effect of the lipid matrix on drug entrapment, in vitro release, and physical stability of olanzapine-loaded solid lipid nanoparticles
resolves10.1208/pt070378
Once-daily tablet formulation and in vitro release evaluation of cefpodoxime using hydroxypropyl methylcellulose: A technical note
resolves10.1208/ps050213
Wet granulation fine particle ethylcellulose tablets: Effect of production variables and mathematical modeling of drug release
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Controlled Release Matrix Tablets of Zidovudine: Effect of Formulation Variables on the In Vitro Drug Release Kinetics
resolves10.1016/j.ijpharm.2005.12.037
Development of a controlled release low dose class II drug-Glipizide
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Mechanisms of solute release from porous hydrophilic polymers
resolves10.1023/A:1011976615750
In Vitro Dissolution Profile Comparison—Statistics and Analysis of the Similarity Factor, f2
resolves10.1208/s12249-010-9380-5
In Vitro Release Kinetics and Bioavailability of Gastroretentive Cinnarizine Hydrochloride Tablet
resolves10.1208/s12248-008-9031-x
Development of a GC-MS Assay for the Determination of Fentanyl Pharmacokinetics in Rabbit Plasma after Sublingual Spray Delivery
resolves10.1208/s12249-007-9031-7
Development and Evaluation of Buccoadhesive Controlled Release Tablets of Lercanidipine
resolves10.1016/S0378-4347(99)00017-1
Determination of olanzapine in human breast milk by high-performance liquid chromatography with electrochemical detection
resolves10.1002/jps.2600531126
Kinetic Analysis of Blood Levels and Urinary Excretion in the Absorptive Phase after Single Doses of Drug
resolves10.1016/S0920-9964(01)00312-7
Predictors of medication discontinuation by patients with first-episode schizophrenia and schizoaffective disorder
resolves10.1002/jps.2600690102
Role of Binders in Moisture-Induced Hardness Increase in Compressed Tablets and its effect on in Vitro Disintegration and Dissolution
resolves10.3109/03639040903025848
Formulation and evaluation of natural gum-based sustained release matrix tablets of flurbiprofen using response surface methodology
resolves10.1016/S0168-3659(00)00366-7
Translocation of drug particles in HPMC matrix gel layer: effect of drug solubility and influence on release rate
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A simple equation for description of solute release II. Fickian and anomalous release from swellable devices
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A simple equation for description of solute release I. Fickian and non-fickian release from non-swellable devices in the form of slabs, spheres, cylinders or discs
resolves10.1016/S0168-3659(99)00004-8
Identification of critical formulation and processing variables for metoprolol tartrate extended-release (ER) matrix tablets1This manuscript represents the personal opinions of the authors and does not necessarily represent the views or policies of the FDA.1
resolves10.1021/js950359z
Influence of pH on the Release of Propranolol Hydrochloride from Matrices Containing Hydroxypropylmethylcellulose K4M and Carbopol 974
resolves10.1248/cpb.54.1091
Analysis of the Release Process of Phenylpropanolamine Hydrochloride from Ethylcellulose Matrix Granules III. Effects of the Dissolution Condition on the Release Process
resolves10.1021/mp034006h
Molecular Properties of WHO Essential Drugs and Provisional Biopharmaceutical Classification
The 5 references without a DOI — listed, not checked
no DOI — not checkedMartindale SS. The complete drug reference. 35th ed. London: The Pharmaceutical Press; 2008.
no DOI — not checkedFDA. Guidance for industry. Dissolution testing of immediate release solid oral dosage forms. Rockville; 1997.
no DOI — not checkedShargel L, Yu A. Bioavailability and bioequivalence. In: Shargel L, Yu AB (eds) Applied biopharmaceutics and pharmacokinetics, 4th ed. New York: McGraw-Hill Medical Publishing Company; 1999.
no DOI — not checkedRowe RC, Sheskey PJ, Owen SC. Handbook of pharmaceutical excipient. London: Pharmaceutical Press; 2006.
no DOI — not checkedPeppas NA. Analysis of Fickian and non-Fickian drug release from polymers. Pharm Acta Helv. 1985;60(4):110–1.
What this badge says. CiteStamped means the CHECKABLE references of this work were clean at the dated check: each resolved to a known work in a public registry, and none carried a retraction notice at that time. It says nothing about the quality, findings, or importance of the work itself, and nothing about references deposited without a DOI.

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