Annealing as a tool for the optimization of lyophilization and ensuring of the stability of protein-loaded PLGA nanoparticles

被引:33
作者
Fonte, Pedro [1 ,2 ,3 ]
Lino, Paulo Roque [4 ]
Seabra, Vitor [2 ,3 ]
Almeida, Antonio J. [4 ]
Reis, Salette [1 ]
Sarmento, Bruno [2 ,3 ,5 ,6 ]
机构
[1] Univ Porto, UCIBIO, REQUIMTE, Fac Pharm,Dept Chem Sci,Appl Chem Lab, Rua Jorge Viterbo Ferreira 228, P-4050113 Oporto, Portugal
[2] CESPU, Inst Invest & Formacao Avancada Ciencias & Tecnol, Rua Cent Gandra 1317, P-4585116 Gandra Prd, Portugal
[3] Inst Univ Ciencias Saude, Rua Cent Gandra 1317, P-4585116 Gandra Prd, Portugal
[4] Univ Lisbon, iMed ULisboa, Fac Pharm, Ave Prof Gama Pinto, P-1649003 Lisbon, Portugal
[5] Univ Porto, i3S, Inst Invest & Inovacao Saude, Rua Jorge Viterbo Ferreira 228, P-4050113 Oporto, Portugal
[6] Univ Porto, INEB Inst Engn Biomed, Rua Alfredo Allen 208, P-4200135 Oporto, Portugal
关键词
Annealing; FTIR; Insulin; Lyophilization; Nanoparticle; Protein; PLGA; PRIMARY DRYING RATE; I INFRARED-SPECTRA; SECONDARY STRUCTURE; INSULIN; NANOCAPSULES; CRYOPROTECTANTS; PHARMACEUTICALS; STABILIZATION; FIBRILLATION; TEMPERATURE;
D O I
10.1016/j.ijpharm.2016.03.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this work was to use annealing as a tool to optimize the lyophilization cycle by decreasing its duration time, and simultaneously preserve the stability of poly( lactic-co-glycolic acid) nanoparticles and with upmost importance, maintain the structural stability of loaded insulin, used as model therapeutic protein. The contribution of a cryoprotectant in this preservation process was also evaluated. Insulin-loaded nanoparticles co-encapsulated with and without trehalose as cryoprotectant were produced, resulting in a particle size of about 250-300 nm, a PdI around 0.25 and a zeta potential in the range of -20 to -24 mV. The insulin association efficiency was higher than 90%, and the loading capacity was of 11-12%. The use of annealing allowed the decrease of duration time of primary drying in about 38%, representing a global decrease of lyophilization time of around 26%. The residual moisture content of all lyophilizates was around 1%, and the reconstitution of lyophilizates obtained using annealing was even faster than those without annealing. The co-encapsulated trehalose better preserved the nanoparticle size throughout the lyophilization process using annealing, compared to formulation containing no cryoprotectant. Fourier-transform infrared spectroscopy showed that the trehalose-containing nanoparticles presented higher insulin structural maintenance, compared to nanoparticles without cryoprotectant, presenting an insulin structural maintenance of 85.3 +/- 0.7% and 86.0 +/- 1.0% for annealing and no annealing, respectively. This formulation also presented the closest structural similarity with native insulin. Interestingly, the structural features of insulin loaded into nanoparticles upon lyophilization with and without annealing were practically identical, showing that annealing had no detrimental effect in insulin structure. Circular dichroism and fluorescence spectroscopy confirmed these results. Overall, this work gave rise to the importance of annealing in decreasing the duration time of lyophilization of protein-loaded poly(lactic-co-glycolic acid) nanoparticles, and simultaneously ensuring the stability of the carrier and loaded protein. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:163 / 173
页数:11
相关论文
共 50 条
[31]   Statistical Design for Formulation Optimization of Hydrocortisone Butyrate-Loaded PLGA Nanoparticles [J].
Yang, Xiaoyan ;
Patel, Sulabh ;
Sheng, Ye ;
Pal, Dhananjay ;
Mitra, Ashim K. .
AAPS PHARMSCITECH, 2014, 15 (03) :569-587
[32]   Taguchi design for optimization and development of antibacterial drug-loaded PLGA nanoparticles [J].
Sonam, Hema Chaudhary ;
Kumar, Vikash .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2014, 64 :99-105
[33]   Statistical Design for Formulation Optimization of Hydrocortisone Butyrate-Loaded PLGA Nanoparticles [J].
Xiaoyan Yang ;
Sulabh Patel ;
Ye Sheng ;
Dhananjay Pal ;
Ashim K. Mitra .
AAPS PharmSciTech, 2014, 15 :569-587
[34]   Stem cell differentiation-related protein-loaded PLGA microspheres as a novel platform micro-typed scaffold for chondrogenesis [J].
Park, Ji Sun ;
Lim, Hye-Jin ;
Yi, Se Won ;
Park, Keun-Hong .
BIOMEDICAL MATERIALS, 2016, 11 (05)
[35]   Preparation, characterization and optimization of sildenafil citrate loaded PLGA nanoparticles by statistical factorial design [J].
Ghasemian, Elham ;
Vatanara, Alireza ;
Najafabadi, Abdolhossein Rouholamini ;
Rouini, Mohammad Reza ;
Gilani, Kambiz ;
Darabi, Majid .
DARU-JOURNAL OF PHARMACEUTICAL SCIENCES, 2013, 21
[36]   Preparation, characterization and optimization of sildenafil citrate loaded PLGA nanoparticles by statistical factorial design [J].
Elham Ghasemian ;
Alireza Vatanara ;
Abdolhossein Rouholamini Najafabadi ;
Mohammad Reza Rouini ;
Kambiz Gilani ;
Majid Darabi .
DARU Journal of Pharmaceutical Sciences, 21
[37]   Cyclosporin A Loaded PLGA Nanoparticle: Preparation, Optimization, In-Vitro Characterization and Stability Studies [J].
Jain, Sanyog ;
Mittal, Ankit ;
Jain, Amit K. ;
Mahajan, Rahul R. ;
Singh, Dinesh .
CURRENT NANOSCIENCE, 2010, 6 (04) :422-431
[38]   Understanding the quality of protein loaded PLGA nanoparticles variability by Plackett-Burman design [J].
Rahman, Ziyaur ;
Zidan, Ahmed S. ;
Habib, Muhammad J. ;
Khan, Mansoor A. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2010, 389 (1-2) :186-194
[39]   Impact of Lipid/Magnesium Hydroxide Hybrid Nanoparticles on the Stability of Vascular Endothelial Growth Factor-Loaded PLGA Microspheres [J].
Omidi, Meisam ;
Mansouri, Vahid ;
Amirabad, Leila Mohammadi ;
Tayebi, Lobat .
ACS APPLIED MATERIALS & INTERFACES, 2021, 13 (21) :24370-24384
[40]   Paeonol-loaded PLGA nanoparticles as an oral drug delivery system: Design, optimization and evaluation [J].
Wang, Fangyuan ;
Shan, Qianqian ;
Chang, Xiangwei ;
Li, Zhenbao ;
Gui, Shuangying .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2021, 602