Three Polymorphs and Two Hydrates of a Multidrug Crystal Involving Gefitinib and Rhein: Characterization, Stability, and Solubility Aspects
Multidrug crystals, comprising multiple drugs in the same crystal lattice, can be used to develop drug combinations with improved physicochemical properties. The investigation on polymorphism of a given multidrug crystal aids in finding the optimal solid form for the development of combined formulat...
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Published in | Crystal growth & design Vol. 24; no. 11; pp. 4501 - 4509 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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American Chemical Society
05.06.2024
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Abstract | Multidrug crystals, comprising multiple drugs in the same crystal lattice, can be used to develop drug combinations with improved physicochemical properties. The investigation on polymorphism of a given multidrug crystal aids in finding the optimal solid form for the development of combined formulations. In this work, three polymorphs (GTB−RH I, GTB−RH II, and GTB−RH III) and two hydrates (GTB−RH·4.25H 2 O and GTB−RH·1.25H 2 O) of a multidrug crystal involving gefitinib (GTB) and rhein (RH) were successfully obtained and fully characterized by X-ray diffraction (XRD), 1H nuclear magnetic resonance (1H NMR), thermogravimetric analysis (TG), differential scanning calorimetry (DSC), Fourier transform infrared (FT-IR), and dynamic vapor sorption (DVS) measurements. Thermal analysis reveals that GTB−RH I and GTB−RH II are monotropically related, while GTB−RH II and GTB−RH III are enantiotropically related. GTB−RH I is a metastable form, GTB−RH II is the stable form at lower temperature, and GTB−RH III is the stable form at higher temperature. The transition of GTB−RH II to GTB−RH III occurs upon heating to 190 °C. Slurry conversion experiments indicate that GTB−RH·4.25H 2 O is the stable form in aqueous solutions, while GTB−RH II is the stable form in nonaqueous solutions. Accelerated stability tests show that GTB−RH·1.25H 2 O and GTB−RH I converted to GTB−RH·4.25H 2 O, while GTB−RH·4.25H 2 O, GTB−RH II, and GTB−RH III remained intact up to three months. In addition, dissolution experiments demonstrate the apparent solubility of GTB and RH in the following order: GTB−RH III > GTB−RH II > GTB−RH I > GTB−RH·1.25H 2 O > GTB−RH·4.25H 2 O. This work shows that GTB−RH III has great potential to be developed into a combined formulation as it exhibits simultaneously and significantly improved solubility for both GTB and RH. |
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AbstractList | Multidrug crystals, comprising multiple drugs in the same crystal lattice, can be used to develop drug combinations with improved physicochemical properties. The investigation on polymorphism of a given multidrug crystal aids in finding the optimal solid form for the development of combined formulations. In this work, three polymorphs (GTB−RH I, GTB−RH II, and GTB−RH III) and two hydrates (GTB−RH·4.25H 2 O and GTB−RH·1.25H 2 O) of a multidrug crystal involving gefitinib (GTB) and rhein (RH) were successfully obtained and fully characterized by X-ray diffraction (XRD), 1H nuclear magnetic resonance (1H NMR), thermogravimetric analysis (TG), differential scanning calorimetry (DSC), Fourier transform infrared (FT-IR), and dynamic vapor sorption (DVS) measurements. Thermal analysis reveals that GTB−RH I and GTB−RH II are monotropically related, while GTB−RH II and GTB−RH III are enantiotropically related. GTB−RH I is a metastable form, GTB−RH II is the stable form at lower temperature, and GTB−RH III is the stable form at higher temperature. The transition of GTB−RH II to GTB−RH III occurs upon heating to 190 °C. Slurry conversion experiments indicate that GTB−RH·4.25H 2 O is the stable form in aqueous solutions, while GTB−RH II is the stable form in nonaqueous solutions. Accelerated stability tests show that GTB−RH·1.25H 2 O and GTB−RH I converted to GTB−RH·4.25H 2 O, while GTB−RH·4.25H 2 O, GTB−RH II, and GTB−RH III remained intact up to three months. In addition, dissolution experiments demonstrate the apparent solubility of GTB and RH in the following order: GTB−RH III > GTB−RH II > GTB−RH I > GTB−RH·1.25H 2 O > GTB−RH·4.25H 2 O. This work shows that GTB−RH III has great potential to be developed into a combined formulation as it exhibits simultaneously and significantly improved solubility for both GTB and RH. |
Author | Ren, Bo-Ying Dai, Xia-Lin Chen, Jia-Mei Zhang, Fang Long, Xiang-Tian Lu, Tong-Bu |
AuthorAffiliation | Tasly Academy, Tasly Holding Group Co., Ltd Tianjin University of Technology School of Chemistry and Chemical Engineering Institute for New Energy Materials and Low Carbon Technologies, School of Materials Science and Engineering |
AuthorAffiliation_xml | – name: Institute for New Energy Materials and Low Carbon Technologies, School of Materials Science and Engineering – name: Tasly Academy, Tasly Holding Group Co., Ltd – name: School of Chemistry and Chemical Engineering – name: Tianjin University of Technology |
Author_xml | – sequence: 1 givenname: Fang surname: Zhang fullname: Zhang, Fang organization: School of Chemistry and Chemical Engineering – sequence: 2 givenname: Xiang-Tian surname: Long fullname: Long, Xiang-Tian organization: Tasly Academy, Tasly Holding Group Co., Ltd – sequence: 3 givenname: Bo-Ying surname: Ren fullname: Ren, Bo-Ying organization: Tianjin University of Technology – sequence: 4 givenname: Xia-Lin orcidid: 0000-0002-8605-6173 surname: Dai fullname: Dai, Xia-Lin organization: School of Chemistry and Chemical Engineering – sequence: 5 givenname: Tong-Bu orcidid: 0000-0002-6087-4880 surname: Lu fullname: Lu, Tong-Bu organization: Tianjin University of Technology – sequence: 6 givenname: Jia-Mei orcidid: 0000-0002-3959-901X surname: Chen fullname: Chen, Jia-Mei email: chenjiamei@email.tjut.edu.cn organization: School of Chemistry and Chemical Engineering |
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Title | Three Polymorphs and Two Hydrates of a Multidrug Crystal Involving Gefitinib and Rhein: Characterization, Stability, and Solubility Aspects |
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