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.
The 42 checked references that resolve
resolves10.1016/j.pnpbp.2005.04.037Safety and effectiveness of olanzapine in monotherapy: A multivariate analysis of a naturalistic study
resolves10.4088/JCP.0207e04Effectiveness of Antipsychotic Drugs in Patients with Chronic Schizophrenia
resolves10.1016/0378-4347(95)00061-MAnalysis of olanzapine in human plasma utilizing reversed-phase high-performance liquid chromatography with electrochemical detection
resolves10.1055/s-2007-973836A Study of Genetic (<i>CYP2D6</i> and <i>ABCB1</i>) and Environmental (Drug Inhibitors and Inducers) Variables That May Influence Plasma Risperidone Levels
resolves10.1111/j.1532-5415.2005.53418.xAntipsychotic Medications and Drug‐Induced Movement Disorders Other Than Parkinsonism: A Population‐Based Cohort Study in Older Adults
resolves10.1176/appi.ps.52.6.805Using Drug Claims Data to Assess the Relationship of Medication Adherence With Hospitalization and Costs
resolves10.1185/030079908X253384Switching from other antipsychotics to once-daily extended release quetiapine fumarate in patients with schizophrenia
resolves10.1208/s12249-008-9108-yFormulation, Release Characteristics and Bioavailability Study of Oral Monolithic Matrix Tablets Containing Carbamazepine
resolves10.1208/pt0804083Investigations of the effect of the lipid matrix on drug entrapment, in vitro release, and physical stability of olanzapine-loaded solid lipid nanoparticles
resolves10.1208/pt070378Once-daily tablet formulation and in vitro release evaluation of cefpodoxime using hydroxypropyl methylcellulose: A technical note
resolves10.1208/ps050213Wet granulation fine particle ethylcellulose tablets: Effect of production variables and mathematical modeling of drug release
resolves10.1208/s12249-007-9030-8Controlled Release Matrix Tablets of Zidovudine: Effect of Formulation Variables on the In Vitro Drug Release Kinetics
resolves10.1002/jps.2600521210Mechanism of sustained‐action medication. Theoretical analysis of rate of release of solid drugs dispersed in solid matrices
resolves10.1023/A:1011976615750In Vitro Dissolution Profile Comparison—Statistics and Analysis of the Similarity Factor, f2
resolves10.1208/s12249-010-9380-5In Vitro Release Kinetics and Bioavailability of Gastroretentive Cinnarizine Hydrochloride Tablet
resolves10.1208/s12248-008-9031-xDevelopment of a GC-MS Assay for the Determination of Fentanyl Pharmacokinetics in Rabbit Plasma after Sublingual Spray Delivery
resolves10.1016/S0378-4347(99)00017-1Determination of olanzapine in human breast milk by high-performance liquid chromatography with electrochemical detection
resolves10.1002/jps.2600531126Kinetic Analysis of Blood Levels and Urinary Excretion in the Absorptive Phase after Single Doses of Drug
resolves10.1016/S0920-9964(01)00312-7Predictors of medication discontinuation by patients with first-episode schizophrenia and schizoaffective disorder
resolves10.1002/jps.2600690102Role of Binders in Moisture-Induced Hardness Increase in Compressed Tablets and its effect on in Vitro Disintegration and Dissolution
resolves10.3109/03639040903025848Formulation and evaluation of natural gum-based sustained release matrix tablets of flurbiprofen using response surface methodology
resolves10.1016/S0168-3659(00)00366-7Translocation of drug particles in HPMC matrix gel layer: effect of drug solubility and influence on release rate
resolves10.1016/0168-3659(87)90035-6A simple equation for description of solute release II. Fickian and anomalous release from swellable devices
resolves10.1016/0168-3659(87)90034-4A 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)00004-8Identification 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/js950359zInfluence of pH on the Release of Propranolol Hydrochloride from Matrices Containing Hydroxypropylmethylcellulose K4M and Carbopol 974
resolves10.1248/cpb.54.1091Analysis of the Release Process of Phenylpropanolamine Hydrochloride from Ethylcellulose Matrix Granules III. Effects of the Dissolution Condition on the Release Process
resolves10.1021/mp034006hMolecular 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.
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