Exploring the chemical space for freeze-drying excipients

Research output: Contribution to journalJournal articleResearchpeer-review

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Exploring the chemical space for freeze-drying excipients. / Meng-Lund, Helena; Holm, Tobias Palle; Poso, Antti; Jorgensen, Lene; Rantanen, Jukka; Grohganz, Holger.

In: International Journal of Pharmaceutics, Vol. 566, 2019, p. 254-263.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Meng-Lund, H, Holm, TP, Poso, A, Jorgensen, L, Rantanen, J & Grohganz, H 2019, 'Exploring the chemical space for freeze-drying excipients', International Journal of Pharmaceutics, vol. 566, pp. 254-263. https://doi.org/10.1016/j.ijpharm.2019.05.065

APA

Meng-Lund, H., Holm, T. P., Poso, A., Jorgensen, L., Rantanen, J., & Grohganz, H. (2019). Exploring the chemical space for freeze-drying excipients. International Journal of Pharmaceutics, 566, 254-263. https://doi.org/10.1016/j.ijpharm.2019.05.065

Vancouver

Meng-Lund H, Holm TP, Poso A, Jorgensen L, Rantanen J, Grohganz H. Exploring the chemical space for freeze-drying excipients. International Journal of Pharmaceutics. 2019;566:254-263. https://doi.org/10.1016/j.ijpharm.2019.05.065

Author

Meng-Lund, Helena ; Holm, Tobias Palle ; Poso, Antti ; Jorgensen, Lene ; Rantanen, Jukka ; Grohganz, Holger. / Exploring the chemical space for freeze-drying excipients. In: International Journal of Pharmaceutics. 2019 ; Vol. 566. pp. 254-263.

Bibtex

@article{25f645315dc54c0dad7f92acf20f7b90,
title = "Exploring the chemical space for freeze-drying excipients",
abstract = "Commonly, a limited number of generally accepted bulking agents and lyoprotectants are used for freeze-drying; predominantly mannitol, glycine, sucrose and trehalose. The purpose of this study was to combine a theoretical approach using molecular descriptors with a large scale experimental screening to evaluate the suitability of a broad range of excipients for freeze-drying. A large selection of sugars, polyols and amino acids was characterized by modulated differential scanning calorimetry (mDSC) and X-ray powder diffraction (XRPD) after well-plate based freeze-drying. The calculated molecular descriptors were investigated with both hierarchical cluster analysis and principal component analysis. A clear clustering of the excipients according to the size-related and weight-related descriptors was observed; however other relevant descriptors could also be identified. From a practical perspective, a trend was observed with regard to a higher likelihood for amorphisation and a higher glass transition temperature of the maximally freeze-concentrated solution with increasing molecular size. A translation of the molecular descriptors on pharmaceutical performance was more successful for lyoprotectants than for bulking agents. Additionally, in the course of the experimental screening, several new potential bulking agents and lyoprotectants were identified.",
author = "Helena Meng-Lund and Holm, {Tobias Palle} and Antti Poso and Lene Jorgensen and Jukka Rantanen and Holger Grohganz",
note = "Copyright {\textcopyright} 2019 Elsevier B.V. All rights reserved.",
year = "2019",
doi = "10.1016/j.ijpharm.2019.05.065",
language = "English",
volume = "566",
pages = "254--263",
journal = "International Journal of Pharmaceutics",
issn = "0378-5173",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Exploring the chemical space for freeze-drying excipients

AU - Meng-Lund, Helena

AU - Holm, Tobias Palle

AU - Poso, Antti

AU - Jorgensen, Lene

AU - Rantanen, Jukka

AU - Grohganz, Holger

N1 - Copyright © 2019 Elsevier B.V. All rights reserved.

PY - 2019

Y1 - 2019

N2 - Commonly, a limited number of generally accepted bulking agents and lyoprotectants are used for freeze-drying; predominantly mannitol, glycine, sucrose and trehalose. The purpose of this study was to combine a theoretical approach using molecular descriptors with a large scale experimental screening to evaluate the suitability of a broad range of excipients for freeze-drying. A large selection of sugars, polyols and amino acids was characterized by modulated differential scanning calorimetry (mDSC) and X-ray powder diffraction (XRPD) after well-plate based freeze-drying. The calculated molecular descriptors were investigated with both hierarchical cluster analysis and principal component analysis. A clear clustering of the excipients according to the size-related and weight-related descriptors was observed; however other relevant descriptors could also be identified. From a practical perspective, a trend was observed with regard to a higher likelihood for amorphisation and a higher glass transition temperature of the maximally freeze-concentrated solution with increasing molecular size. A translation of the molecular descriptors on pharmaceutical performance was more successful for lyoprotectants than for bulking agents. Additionally, in the course of the experimental screening, several new potential bulking agents and lyoprotectants were identified.

AB - Commonly, a limited number of generally accepted bulking agents and lyoprotectants are used for freeze-drying; predominantly mannitol, glycine, sucrose and trehalose. The purpose of this study was to combine a theoretical approach using molecular descriptors with a large scale experimental screening to evaluate the suitability of a broad range of excipients for freeze-drying. A large selection of sugars, polyols and amino acids was characterized by modulated differential scanning calorimetry (mDSC) and X-ray powder diffraction (XRPD) after well-plate based freeze-drying. The calculated molecular descriptors were investigated with both hierarchical cluster analysis and principal component analysis. A clear clustering of the excipients according to the size-related and weight-related descriptors was observed; however other relevant descriptors could also be identified. From a practical perspective, a trend was observed with regard to a higher likelihood for amorphisation and a higher glass transition temperature of the maximally freeze-concentrated solution with increasing molecular size. A translation of the molecular descriptors on pharmaceutical performance was more successful for lyoprotectants than for bulking agents. Additionally, in the course of the experimental screening, several new potential bulking agents and lyoprotectants were identified.

U2 - 10.1016/j.ijpharm.2019.05.065

DO - 10.1016/j.ijpharm.2019.05.065

M3 - Journal article

C2 - 31145963

VL - 566

SP - 254

EP - 263

JO - International Journal of Pharmaceutics

JF - International Journal of Pharmaceutics

SN - 0378-5173

ER -

ID: 221824845