Comparative analysis of polystyrene versus zirconia beads on breakage kinetics, heat generation, and amorphous formation during wet bead milling

被引:0
作者
Guner, Gulenay [1 ]
Heidari, Hamidreza [2 ]
Lehman, Kaitlyn [1 ]
Desai, Parind M. [1 ]
Clancy, Donald [1 ]
Bilgili, Ecevit [2 ]
Chattoraj, Sayantan [1 ]
机构
[1] GlaxoSmithKline Res & Dev Ltd, Drug Prod Dev, Med Dev & Supply, Collegeville, PA 19426 USA
[2] New Jersey Inst Technol, Otto H York Dept Chem & Mat Engn, Newark, NJ 07102 USA
关键词
Milling; Processing; Nanoparticles; Suspensions; Mathematical model; Dynamic simulation; Particle sizing; Raman spectroscopy; Amorphous; DRUG NANOSUSPENSIONS; MEDIA; DELIVERY;
D O I
10.1016/j.xphs.2024.11.029
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This study determined process conditions under which polystyrene (CPS) and zirconia (YSZ) beads cause similar breakage kinetics and temperature rise during manufacturing of drug nanosuspensions via wet bead milling and explored relative advantages of CPS beads, particularly for stress-sensitive compounds. Besides temperature and particle size measurements, a microhydrodynamic-based kinetic model simulated the conditions for CPS to achieve breakage rates equivalent to those of YSZ. A power law correlation was applied to find conditions conducive to temperature equivalency. The maximum contact pressure and pseudo energy dissipation rate were calculated under these equivalency conditions. When bead loading for CPS was increased to match with YSZ, lower temperature at similar breakage conditions or faster breakage at the same temperature was achieved. Increasing the tip speed did not provide any notable advantages for CPS over YSZ in terms of breakage kinetics or temperature. However, under all conditions investigated, CPS beads exhibited markedly lower maximum contact pressure and pseudo energy dissipation rate, which may correlate with reduced mechanically induced amorphization during milling. A proof-of-concept study demonstrated that a mechanical stress-sensitive drug had lower amorphous generation with CPS compared to YSZ. Therefore, CPS beads are a promising alternative to YSZ beads, especially when used at the highest feasible loading.<br /> (c) 2024 American Pharmacists Association. Published by Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
引用
收藏
页码:1175 / 1185
页数:11
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共 42 条
  • [11] Halpern V., Stalter R.M., Owen D.H., Dorflinger L.J., Lendvay A., Rademacher K.H., Towards the development of a longer-acting injectable contraceptive: past research and current trends, Contraception, 92, 1, pp. 3-9, (2015)
  • [12] Bassand C., Villois A., Gianola L., Et al., Smart design of patient-centric long-acting products: from preclinical to marketed pipeline trends and opportunities, Expert Opin Drug Deliv, 19, 10, pp. 1265-1283, (2022)
  • [13] Jog R., Burgess D.J., Comprehensive quality by design approach for stable nanocrystalline drug products, Int J Pharm, 564, pp. 426-460, (2019)
  • [14] Kumar A., Sahu R., Tripathy S.K., Energy-efficient advanced ultrafine grinding of particles using stirred mills—a review, Energies, 16, 14, (2023)
  • [15] Mura P.A., Cirri M., Rossetti A., Allemandi D.A., Paredes A.J., Palma S.D., Preparation of glyburide nanocrystals with improved dissolution properties by dry-ball- and wet-bead- milling: systematic comparison by experimental design of the performance of the two methods, J Drug Deliv Sci Technol, 91, (2024)
  • [16] Merisko-Liversidge E., Liversidge G.G., Nanosizing for oral and parenteral drug delivery: a perspective on formulating poorly-water soluble compounds using wet media milling technology, Adv Drug Deliv Rev, 63, 6, pp. 427-440, (2011)
  • [17] Guner G., Kannan M., Berrios M., Bilgili E., Use of bead mixtures as a novel process optimization approach to nanomilling of drug suspensions, Pharm. Res., 38, 7, pp. 1279-1296, (2021)
  • [18] Guner G., Elashri S., Mehaj M., Et al., An enthalpy-balance model for timewise evolution of temperature during wet stirred media milling of drug suspensions, Pharm Res, 39, pp. 2065-2082, (2022)
  • [19] Guner G., Seetharaman N., Elashri S., Mehaj M., Bilgili E., Analysis of heat generation during the production of drug nanosuspensions in a wet stirred media mill, Int J Pharm, 624, (2022)
  • [20] Kwade A., Schwedes J., Wet grinding in stirred media mills, Handb Powder Technol, 12, pp. 251-382, (2007)