Skip to main content
Log in

Water and the relationship to the crystal structure stability of azithromycin

Thermal investigations of solvatomorphism, amorphism and polymorphism

  • Published:
Journal of Thermal Analysis and Calorimetry Aims and scope Submit manuscript

Abstract

This study investigated the solid-state physical stabilities of azithromycin dihydrate (AZM-DH), thermally prepared anhydrate and hemihydrate modifications. Programmed thermal treatment of AZM-DH in DSC yielded the formation of anhydrate amorphs (I, II), crystalline AZM anhydrate and hemihydrate phases. The formation of the anhydrate amorphs, I and II, respectively, involved different transformation pathways of solid–liquid–solid (melting and supercooling) and solid–solid (378 K for 24 h.). Both amorph phases exhibit hygroscopic behaviour, producing non-stoichiometric hydrates, with extent of moisture absorption increasing with increased storage humidity (0–96% RH/313 K). TG analysis after controlled storage (4 days at 96% RH/313 K) detected absorbed waters of hydration up to 5.9 and 5.3% for amorphs I and II, respectively. The crystal anhydrate and hemihydrate phases were hygroscopic and readily converted to the stoichiometric dihydrate form, which was compositionally stable in RH ranges from 11 to 96% at 313 K. Solubility studies, performed in distilled water at 310 K, showed an at least 1.5 fold solubility improvement for both amorph forms relative to crystalline AZM-DH, but with some evidence of solvent-mediated phase transformation after 20 min. Structural characterization by single-crystal XRD concluded that thermally stimulated amorphization required energy to disrupt intermolecular hydrogen bond interactions by bridging water molecules in addition to hydrogen bond interactions between neighbouring AZM molecules in unit cell.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8

Similar content being viewed by others

References

  1. Vippagunta SR, Brittain HG, Grant DJW. Crystalline solids. Adv Drug Deliv Rev. 2001;48:3–26.

    Article  CAS  Google Scholar 

  2. Qu H, Louhi-Kultanen M, Kallas J. Solubility and stability of anhydrate/hydrate in solvent mixtures. Int J Pharm. 2006;321:101–7.

    Article  CAS  Google Scholar 

  3. Schartman RR. On the thermodynamics of cocrystal formation. Int J Pharm. 2009;365(1–2):77–80.

    Article  CAS  Google Scholar 

  4. Schatzberg P. Molecular diameter of water from solubility and diffusion measurements. J Phys Chem. 1967;71(13):4569–70.

    Article  CAS  Google Scholar 

  5. Morris KR. Structural aspects of hydrates and solvates. Brittain HG, Editor, Polymorphism in pharmaceutical solids. New York: Marcell Dekker 1999;95:125–81.

  6. Wang SL, Wong YC, Cheng WT, Lin SY. A continuous process for solid-state dehydration, amorphization and recrystallization of metoclopramide HCL monohydrate studied by simultaneous DSC-FTIR microspectroscopy. J Therm Anal Calorim. 2011;104(1):261–4.

    Article  CAS  Google Scholar 

  7. Einfalt T, Planinšek O, Hrovat K. Methods of amorphization and investigation of the amorphous state. Acta Pharm. 2013;63(3):305–34.

    Article  CAS  Google Scholar 

  8. Surana R, Pyne A, Suryanarayanan R. Effect of preparation method on physical properties of amorphous trehalose. Pharm Res. 2003;21(7):1167–76.

    Article  Google Scholar 

  9. Healy AM, Worku ZA, Kumar D, Madi AM. Pharmaceutical solvates, hydrates and amorphous forms: A special emphasis on cocrystals. Adv Drug Del Rev. 2017 in press.

  10. Hof H. Macrolides, a group of antibiotics with a broad spectrum of activity. Immun Infekt. 1994;22(2):66–71.

    CAS  Google Scholar 

  11. Gandhi R, Pillai O, Thilagavathi R, Gopalakrishnan B, Kaul CL, Panchagnula R. Characterization of azithromycin hydrates. Eur J Pharm Sci. 2002;16(3):175–84.

    Article  CAS  Google Scholar 

  12. Timoumi S, Mangin D, Peczalski R, Zagrouba F, Andrieu J. Stability and thermophysical properties of azithromycin dihydrate. Arab J Chem. 2014;7(2):189–95.

    Article  CAS  Google Scholar 

  13. Sundaramurthi P, Suryanarayanan R. Azithromycin hydrates- Implications of processing-induced phase transformations. J Pharm Sci. 2014;103(10):3095–106.

    Article  CAS  Google Scholar 

  14. APEX 2, SADABS and SAINT, Bruker AXS Inc., Madison, Wisconsin, USA, 2010.

  15. Sheldrick GM. A short history of SHELX. Acta Cryst. 2008;A64:112–22.

    Article  Google Scholar 

  16. Hübschle CB, Sheldrick GM, Dittrich B. ShelXle: a Qt graphical user interface for SHELXL. J Appl Cryst. 2011;44:1281–4.

    Article  Google Scholar 

  17. Odendaal RW, Liebenberg W, Aucamp ME. A novel reversed-phase LC method for quantitative detection of azithromycin in bulk drug and tablet formulations in various aqueous media. Pharmazie. 2012;67:984–6.

    CAS  Google Scholar 

  18. Djokic S, Kobrehel G, Lopotar N, Kamenar B, Nagl A, Mrvos D. Erythromycin series part 13. Synthesis and structure elucidation of 10-dihydro-10-deoxo-11-methyl-11-azaerythromycin A. J Chem Res. 1988;1988:152–3.

    Google Scholar 

Download references

Acknowledgements

National Research Foundation (NRF) and Nelson Mandela Metropolitan University (NMMU) for research funding.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to D. Grooff.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (DOCX 516 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Neglur, R., Hosten, E., Aucamp, M. et al. Water and the relationship to the crystal structure stability of azithromycin. J Therm Anal Calorim 132, 373–384 (2018). https://doi.org/10.1007/s10973-017-6928-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10973-017-6928-6

Keywords

Navigation