Strategies for non-invasive delivery of biologics

被引:51
作者
Chung, Seung Woo [2 ]
Hil-lal, Taslim A. [2 ]
Byun, Youngro [1 ,2 ]
机构
[1] Seoul Natl Univ, Dept Mol Med & Biopharmaceut Sci, Grad Sch Convergent Sci & Technol, Seoul 151742, South Korea
[2] Seoul Natl Univ, Coll Pharm, Res Inst Pharmaceut Sci, Seoul 151742, South Korea
关键词
Drug delivery; biologic; macromolecule; oral; pulmonary; nasal; IN-VIVO EVALUATION; ORAL INSULIN DELIVERY; TRIMETHYL CHITOSAN CHLORIDE; MOLECULAR-WEIGHT HEPARIN; CELL-PENETRATING PEPTIDES; HUMAN GROWTH-HORMONE; PULMONARY DRUG-DELIVERY; GLUCAGON-LIKE PEPTIDE-1; POLYMERIC ABSORPTION ENHANCER; RAT ALVEOLAR MACROPHAGES;
D O I
10.3109/1061186X.2012.693499
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Macromolecular therapeutics, in particular, many biologics, is the most advancing category of drugs over conventional chemical drugs. The potency and specificity of the biologics for curing certain disease made them to be a leading compound in the pharmaceutical industry. However, due to their intrinsic nature, including high molecular weight, hydrophilicity and instability, they are difficult to be administered via non-invasive route. This is a major quest especially in biologics, as they are frequently used clinically for chronic disorders, which requires long-term administration. Therefore, many efforts have been made to develop formulation for non-invasive administration, in attempt to improve patient compliance and convenience. In this review, strategies for non-invasive delivery, in particular, oral, pulmonary and nasal delivery, that are recently adopted for delivery of biologics are discussed. Insulin, calcitonin and heparin were mainly focused for the discussion as they could represent protein, polypeptide and polysaccharide drugs, respectively. Many recent attempts for non-invasive delivery of biologics are compared to provide an insight of developing successful delivery system.
引用
收藏
页码:481 / 501
页数:21
相关论文
共 263 条
[61]  
EPPSTEIN DA, 1988, CRC CR REV THER DRUG, V5, P99
[62]   MEASUREMENT OF GASTROINTESTINAL PH PROFILES IN NORMAL AMBULANT HUMAN-SUBJECTS [J].
EVANS, DF ;
PYE, G ;
BRAMLEY, R ;
CLARK, AG ;
DYSON, TJ ;
HARDCASTLE, JD .
GUT, 1988, 29 (08) :1035-1041
[63]   Enhancement of bronchial octreotide absorption by chitosan and N-trimethyl chitosan shows linear in vitro/in vivo correlation [J].
Florea, BI ;
Thanou, M ;
Junginger, HE ;
Borchard, G .
JOURNAL OF CONTROLLED RELEASE, 2006, 110 (02) :353-361
[64]   In vivo evaluation of an oral delivery system for P-gp substrates based on thiolated chitosan [J].
Foeger, Florian ;
Schmitz, Thierry ;
Bernkop-Schnuerch, Andreas .
BIOMATERIALS, 2006, 27 (23) :4250-4255
[65]   Challenges in inhaled product development and opportunities for open innovation [J].
Forbes, Ben ;
Asgharian, Bahman ;
Dailey, Lea Ann ;
Ferguson, Douglas ;
Gerde, Per ;
Gumbleton, Mark ;
Gustavsson, Lena ;
Hardy, Colin ;
Hassall, David ;
Jones, Rhys ;
Lock, Ruth ;
Maas, Janet ;
McGovern, Tim ;
Pitcairn, Gary R. ;
Somers, Graham ;
Wolff, Ron K. .
ADVANCED DRUG DELIVERY REVIEWS, 2011, 63 (1-2) :69-87
[66]   Protein drug stability: A formulation challenge [J].
Frokjaer, S ;
Otzen, DE .
NATURE REVIEWS DRUG DISCOVERY, 2005, 4 (04) :298-306
[67]   Arginine-rich peptides - An abundant source of membrane-permeable peptides having potential as carriers for intracellular protein delivery [J].
Futaki, S ;
Suzuki, T ;
Ohashi, W ;
Yagami, T ;
Tanaka, S ;
Ueda, K ;
Sugiura, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (08) :5836-5840
[68]   Lectin-mediated drug delivery: binding and uptake of BSA-WGA conjugates using the Caco-2 model [J].
Gabor, F ;
Schwarzbauer, A ;
Wirth, M .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 237 (1-2) :227-239
[69]   ALGINATES [J].
GACESA, P .
CARBOHYDRATE POLYMERS, 1988, 8 (03) :161-182
[70]   Improvement of intestinal absorption of water-soluble macromolecules by various polyamines: Intestinal mucosal toxicity and absorption-enhancing mechanism of spermine [J].
Gao, Yang ;
He, Lin ;
Katsumi, Hidemasa ;
Sakane, Toshiyasu ;
Fujita, Takuya ;
Yamamoto, Akira .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2008, 354 (1-2) :126-134