Freeze drying of human serum albumin (HSA) nanoparticles with different excipients

被引:97
作者
Anhorn, Marion G. [1 ]
Mahler, Hanns-Christian [1 ]
Langer, Klaus [1 ]
机构
[1] Univ Frankfurt, Bioctr, Inst Pharmaceut Technol, D-60438 Frankfurt, Germany
关键词
Nanoparticles; Human serum albumin (HSA); Lyophilisation; Doxorubicin; Poly(ethylene glycol); Freeze drying;
D O I
10.1016/j.ijpharm.2008.07.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Freeze drying is a suitable technique to improve the long-term storage stability of colloidal drug carrier systems such as nanoparticles. Aim of this study was to systematically evaluate excipients for the freeze drying and long-term stability of albumin-based nanoparticles. In our study, nanoparticles made of human serum albumin (HSA) were freeze dried in the presence of different cryoprotective agents and after reconstitution were evaluated with regard to their physico-chemical characteristics. Empty, doxorubicin-loaded, and PEGylated nanoparticles were prepared and were freeze dried in the presence of different concentrations of sucrose, trehalose, and mannitol, respectively. The samples were physicochemically characterised with regard to lyophilisate appearance, particle size, and polydispersity using photon correlation spectroscopy. For evaluation of long-term stability, the samples were stored at 2-8, 25, and 40 degrees C over predetermined time intervals. In the absence of cryoprotectants, particle growth was observed in all freeze-dried formulations. In the presence of sucrose, mannitol, and trehalose aggregation of HSA nanoparticles during the freeze-drying procedure was prevented. Although all of the excipients were identified to be Suitable stabilisers for freeze drying of HSA nanoparticles, Sucrose and trehalose were superior to mannitol, especially with regard to the long-term storage stability results. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:162 / 169
页数:8
相关论文
共 35 条
[1]  
Akasaka Y, 1988, Drug Des Deliv, V3, P85
[2]  
ALLEMANN E, 1993, EUR J PHARM BIOPHARM, V39, P173
[3]   Colloidal drug carriers: achievements and perspectives [J].
Barratt, G .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2003, 60 (01) :21-37
[4]   Nanoparticle and targeted systems for cancer therapy [J].
Brannon-Peppas, L ;
Blanchette, JO .
ADVANCED DRUG DELIVERY REVIEWS, 2004, 56 (11) :1649-1659
[5]   Rational design of stable lyophilized protein formulations: Some practical advice [J].
Carpenter, JF ;
Pikal, MJ ;
Chang, BS ;
Randolph, TW .
PHARMACEUTICAL RESEARCH, 1997, 14 (08) :969-975
[6]   Mechanism of protein stabilization by sugars during freeze-drying and storage: Native structure preservation, specific interaction, and/or immobilization in a glassy matrix? [J].
Chang, LQ ;
Shepherd, D ;
Sun, J ;
Ouellette, D ;
Grant, KL ;
Tang, XL ;
Pikal, MJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2005, 94 (07) :1427-1444
[7]   Effect of sorbitol and residual moisture on the stability of lyophilized antibodies: Implications for the mechanism of protein stabilization in the solid state [J].
Chang, LQ ;
Shepherd, D ;
Sun, J ;
Tang, XL ;
Pikal, MJ .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2005, 94 (07) :1445-1455
[8]   Partially crystalline systems in lyophilization: I. Use of ternary state diagrams to determine extent of crystallization of bulking agent [J].
Chatterjee, K ;
Shalaev, EY ;
Suryanarayanan, R .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2005, 94 (04) :798-808
[9]  
Costantino H.R, 2004, LYOPHILIZATION BIOPH, V2, P139
[10]   Is trehalose special for preserving dry biomaterials? [J].
Crowe, LM ;
Reid, DS ;
Crowe, JH .
BIOPHYSICAL JOURNAL, 1996, 71 (04) :2087-2093