Formulation Optimization of Freeze-Dried Long-Circulating Liposomes and In-Line Monitoring of the Freeze-Drying Process Using an NIR Spectroscopy Tool

被引:46
作者
Sylvester, Bianca [1 ]
Porfire, Alina [1 ]
Van Bockstal, Pieter-Jan [2 ]
Porav, Sebastian [3 ]
Achim, Marcela [1 ]
De Beer, Thomas [2 ]
Tomuta, Ioan [1 ]
机构
[1] Univ Med & Pharm Iuliu Hatieganu, Dept Pharmaceut Technol & Biopharmaceut, Cluj Napoca, Romania
[2] Univ Ghent, Dept Pharmaceut Anal, Lab Pharmaceut Proc Analyt Technol, Ghent, Belgium
[3] Natl Inst Res & Dev Isotop & Mol Technol, Cluj Napoca, Romania
关键词
liposomes; freeze drying/lyophilization; near-infrared spectroscopy; principal component analysis; encapsulation; process analytical technology (PAT); NEAR-INFRARED SPECTROSCOPY; PHASE-TRANSITION TEMPERATURE; LYOPHILIZATION PROCESS; TERM STABILITY; STABILIZATION; STATE; PHOSPHATIDYLCHOLINE; VITRIFICATION; CHOLESTEROL; QUANTIFICATION;
D O I
10.1016/j.xphs.2017.05.024
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The effect of lyoprotectant type and concentration on the stability of freeze-dried prednisolone sodium phosphate-loaded long-circulating liposomes was investigated. Trehalose at a 5: 1 carbohydrate to lipid molar ratio proved to be superior in maintaining the structural integrity and the permeability properties of the liposome bilayers, assuring the desired characteristics of the final product: a cake with a porous structure and easy to reconstitute, a similar size to the liposomes before freeze-drying, a high percent of encapsulated drug, and a low residual moisture content. Further on, the study demonstrated the possibility of near-infrared spectroscopy to provide valuable insights for detecting critical changes in acyl chain packing of the liposome bilayer. By visualizing the spectra after principal component analysis, one can predict if any harm has occurred to liposome integrity during the process. Moreover, near-infrared spectroscopy enabled us to determine the end points of primary and secondary drying without disturbing the normal freeze-drying procedure, which allowed us to gain a better understanding of the process and to improve process efficiency by optimizing the primary and secondary drying time. (c) 2018 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:139 / 148
页数:10
相关论文
共 59 条
[1]   Freeze-drying of nanoparticles: Formulation, process and storage considerations [J].
Abdelwahed, Wassim ;
Degobert, Ghania ;
Stainmesse, Serge ;
Fessi, Hatem .
ADVANCED DRUG DELIVERY REVIEWS, 2006, 58 (15) :1688-1713
[2]   Preparation and characterization of lyophilized liposomes with incorporated quercetin [J].
Alexopoulou, E ;
Georgopoulos, A ;
Kagkadis, KA ;
Demetzos, C .
JOURNAL OF LIPOSOME RESEARCH, 2006, 16 (01) :17-25
[3]   Stabilization of lipid/DNA complexes during the freezing step of the lyophilization process: the particle isolation hypothesis [J].
Allison, SD ;
Molina, MDC ;
Anchordoquy, TJ .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2000, 1468 (1-2) :127-138
[4]   Nanoparticle dispersity in toxicology [J].
Baalousha, Mohammed ;
Lead, Jamie R. .
NATURE NANOTECHNOLOGY, 2013, 8 (05) :308-309
[5]   Liposomal glucocorticoids as tumor-targeted anti-angiogenic nanomedicine in B16 melanoma-bearing mice [J].
Banciu, Manuela ;
Metselaar, Josbert M. ;
Schiffelers, Raymond M. ;
Storm, Gert .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2008, 111 (1-2) :101-110
[6]   DIFFUSION OF UNIVALENT IONS ACROSS LAMELLAE OF SWOLLEN PHOSPHOLIPIDS [J].
BANGHAM, AD ;
STANDISH, MM ;
WATKINS, JC .
JOURNAL OF MOLECULAR BIOLOGY, 1965, 13 (01) :238-+
[7]  
BARDAT A, 1993, J PARENT SCI TECHN, V47, P293
[8]   Protein stability during freezing: Separation of stresses and mechanisms of protein stabilization [J].
Bhatnagar, Bakul S. ;
Bogner, Robin H. ;
Pikal, Michael J. .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2007, 12 (05) :505-523
[9]   In-situ near-infrared spectroscopy monitoring of the lyophilization process [J].
Brülls, M ;
Folestad, S ;
Sparén, A ;
Rasmuson, A .
PHARMACEUTICAL RESEARCH, 2003, 20 (03) :494-499
[10]   Low amounts of sucrose are sufficient to depress the phase transition temperature of dry phosphatidylcholine, but not for lyoprotection of liposomes [J].
Cacela, C ;
Hincha, DK .
BIOPHYSICAL JOURNAL, 2006, 90 (08) :2831-2842