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Anti-solvent co-crystallization of carbamazepine and saccharin

https://doi.org/10.1016/j.ijpharm.2013.04.012
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36/36 checkable references clean · checked 2026-07-23

Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.

2 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.

The 36 checked references that resolve
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Co-Crystals of the Anti-HIV Drugs Lamivudine and Zidovudine
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Characterization of Carbamazepine-Nicatinamide Cocrystal Polymorphs with Rapid Heating DSC and XRPD
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Selecting the Desired Solid Form by Membrane Crystallizers: Crystals or Cocrystals
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Formation Kinetics and Stability of Carbamazepine−Nicotinamide Cocrystals Prepared by Mechanical Activation
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Particle engineering using sonocrystallization: Salbutamol sulphate for pulmonary delivery
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Crystal Engineering of the Composition of Pharmaceutical Phases:  Multiple-Component Crystalline Solids Involving Carbamazepine
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Cocrystal Formation in Solution: <i>In Situ</i> Solute Concentration Monitoring of the Two Components and Kinetic Pathways
resolves10.1016/j.jcrysgro.2010.12.027
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Performance comparison of a co-crystal of carbamazepine with marketed product
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Cocrystal Formation during Cogrinding and Storage is Mediated by Amorphous Phase
resolves10.1016/j.ijpharm.2012.04.027
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resolves10.1007/s11095-006-9032-3
Use of a Glutaric Acid Cocrystal to Improve Oral Bioavailability of a Low Solubility API
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Phase Solubility Diagrams of Cocrystals Are Explained by Solubility Product and Solution Complexation
resolves10.1016/j.ejps.2009.05.010
Formation of indomethacin–saccharin cocrystals using supercritical fluid technology
resolves10.1021/cg701022e
Polymorphism in Carbamazepine Cocrystals
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Direct production of carbamazepine–saccharin cocrystals from water/ethanol solvent mixtures by membrane-based crystallization technology
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resolves10.1016/j.ejpb.2006.12.002
Influence of sample characteristics on quantification of carbamazepine hydrate formation by X-ray powder diffraction and Raman spectroscopy
resolves10.1002/jps.20756
Influence of Polymorphic Form, Morphology, and Excipient Interactions on the Dissolution of Carbamazepine Compacts
resolves10.1021/mp070001z
An Overview of Pharmaceutical Cocrystals as Intellectual Property
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Simultaneous DSC-FTIR microspectroscopy used to screen and detect the co-crystal formation in real time
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Estimation of Initial Dissolution Rate of Drug Substance by Thermal Analysis: Application for Carbamazepine Hydrate
The 2 references without a DOI — listed, not checked
no DOI — not checkedFDA, 2011. Guidance for industry; Regulatory classification of pharmaceutical co-crystals, http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/default.htm.
no DOI — not checkedPharmaceutical co-crystals – a review
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