Preparation and Spectroscopic Characterization of Inclusion Complexes of 3D Ball-Milled Rifampicin with β-cyclodextrin and γ-cyclodextrin : 3D Ball-Milled Rifampicin with β-cyclodextrin and γ-cyclodextrin
- PMID: 35534746
- DOI: 10.1208/s12249-022-02290-0
Preparation and Spectroscopic Characterization of Inclusion Complexes of 3D Ball-Milled Rifampicin with β-cyclodextrin and γ-cyclodextrin : 3D Ball-Milled Rifampicin with β-cyclodextrin and γ-cyclodextrin
Abstract
Rifampicin (RFP) solutions, intended to reduce incidence of prosthetic graft infection, were prepared as three-dimensional ground mixtures (3DGMs) using β-cyclodextrin (βCD) and γ-cyclodextrin (γCD) and characterized for their spectroscopic properties and solubility. Phase solubility diagrams revealed that 3DGMs (RFP/βCD and RFP/γCD) produced a complex at 1:1 molar ratio. Pulsed field gradient nuclear magnetic resonance experiments indicated that the diffusion coefficients for RFP/βCD and RFP/γCD were similar to the respective diffusion coefficients for βCD and γCD. Rotating-frame Overhauser effect spectroscopy NMR spectra revealed the existence of a new exchanger peak for RFP/γCD, suggesting an intermolecular interaction different from that of RFP/βCD. Differential scanning calorimetry confirmed the presence of endothermic peak at 191 °C indicating the manifestation of RFP in the inclusion complex. Interestingly, molecular interactions from the complexes, RFP/βCD and RFP/γCD, revealed different patterns of inclusion in the 3DGMs. In RFP/βCD, nuclear Overhauser effect spectroscopy NMR spectra indicated cross peaks for the protons of the methyl group of RFP and the protons (H-5 and H-6) in the βCD cavity. The methyl group of RFP interacted with the narrow rim of βCD. With RFP/γCD, cross peaks were due to the protons of the methyl group of RFP and the protons of the cavity of γCD suggesting multiple inclusion patterns. The observed multiple cross peaks affirm the inclusion of RFP into the CD cavity which enhanced its solubility by 1.6-2.0-fold when prepared as 3DGMs as RFP/βCD and RFP/γCD, respectively.
Keywords: 3-dimensionally ground mixture; NMR; Rifampicin; cyclodextrin; inclusion complex; solubility.
© 2022. The Author(s), under exclusive licence to American Association of Pharmaceutical Scientists.
Similar articles
-
Improvement of the Solubility and Evaluation of the Physical Properties of an Inclusion Complex Formed by a New Ferulic Acid Derivative and γ-Cyclodextrin.ACS Omega. 2020 May 18;5(21):12073-12080. doi: 10.1021/acsomega.0c00277. eCollection 2020 Jun 2. ACS Omega. 2020. PMID: 32548386 Free PMC article.
-
Preparation, Characterization, and In Vitro Evaluation of Inclusion Complexes Formed between S-Allylcysteine and Cyclodextrins.ACS Omega. 2022 Aug 24;7(35):31233-31245. doi: 10.1021/acsomega.2c03489. eCollection 2022 Sep 6. ACS Omega. 2022. PMID: 36092555 Free PMC article.
-
Inclusion Complexes of Rifampicin with Native and Derivatized Cyclodextrins: In Silico Modeling, Formulation, and Characterization.Pharmaceuticals (Basel). 2021 Dec 24;15(1):20. doi: 10.3390/ph15010020. Pharmaceuticals (Basel). 2021. PMID: 35056077 Free PMC article.
-
γ-Cyclodextrin.Int J Pharm. 2017 Jan 10;516(1-2):278-292. doi: 10.1016/j.ijpharm.2016.10.062. Epub 2016 Oct 29. Int J Pharm. 2017. PMID: 27989822 Review.
-
Effect of beta-cyclodextrin and hydroxypropyl beta-cyclodextrin complexation on physicochemical properties and antimicrobial activity of cefdinir.J Pharm Biomed Anal. 2008 Jul 15;47(3):535-40. doi: 10.1016/j.jpba.2008.02.006. Epub 2008 Feb 15. J Pharm Biomed Anal. 2008. PMID: 18367363 Review.
Cited by
-
Characterization, Preparation, and Promotion of Plant Growth of 1,3-Diphenylurea/β-Cyclodextrin Derivatives Inclusion Complexes.ACS Omega. 2023 Sep 13;8(38):34972-34981. doi: 10.1021/acsomega.3c04428. eCollection 2023 Sep 26. ACS Omega. 2023. PMID: 37779935 Free PMC article.
-
Nanofibers of Glycyrrhizin/Hydroxypropyl-β-Cyclodextrin Inclusion Complex: Enhanced Solubility Profile and Anti-inflammatory Effect of Glycyrrhizin.AAPS PharmSciTech. 2023 Oct 2;24(7):196. doi: 10.1208/s12249-023-02662-0. AAPS PharmSciTech. 2023. PMID: 37783948
References
-
- Sasashima T, Koshiko S, Muraki S, Nobuyoshi A, Kohsuke Y, Chiba K, Mineji T, Inaba M. Limitations in the use of rifampicin-gelatin grafts against virulent organisms. Surgical Therapy. 2003;88:384–5.
-
- Honig S, Seeger P, Rohde H, Kölbel T, Debus ES, Diener H. Efficacy of antiseptic impregnation of aortic endografts with rifampicin compared to silver against in vitro contamination with four bacteria that frequently cause vascular graft infections. JVS Vasc Sci. 2020;11(1):181–9. - DOI
-
- Uchida N, Katayama A, Tamura K, Miwa S, Masatsugu K, Sueda T. In situ replacement for mycotic aneurysms on the thoracic and abdominal aorta using rifampicin-bonded grafting and omental pedicle grafting. Ann Thorac Surg. 2012;93(2):438–42. - DOI
-
- Coors EA, Seybold H, Merk HF, Mahler V. Polysorbate 80 in medical products and nonimmunologic anaphylactoid reactions. Ann Allergy Asthma Immunol. 2005;95(6):593–9. - DOI
-
- Schwartzberg LS, Navari RM. Safety of polysorbate 80 in the oncology setting. Adv Ther. 2018;35(6):754–67. - DOI
MeSH terms
Substances
LinkOut - more resources
Full Text Sources