Current status and perspectives of biopharmaceutical drugs

被引:28
作者
Ryu, Jae Kuk [1 ]
Kim, Hyo Sun [2 ]
Nam, Doo Hyun [2 ]
机构
[1] Hanmi Pharmaceut Co Ltd, Cent Res Ctr, Dongtan 445813, Hwaseong, South Korea
[2] Yeungnam Univ, Coll Pharm, Gyongsan 712749, South Korea
关键词
biopharmaceutical drug; biosimilar; biobetter; glycoengineering; pegylation; protein engineering; display technology; PREVIOUSLY UNTREATED PATIENTS; RED-CELL APLASIA; SIMILAR BIOTHERAPEUTIC PRODUCTS; RECOMBINANT FACTOR-VIII; ACID ALPHA-GLUCOSIDASE; FACTOR-IX INHIBITORS; GM-CSF ANTIBODIES; TERM-FOLLOW-UP; NEUTRALIZING ANTIBODIES; INTERFERON ALPHA-2A;
D O I
10.1007/s12257-012-0095-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Since the first approval of recombinant human insulin three decades ago, more than 150 biopharmaceutical drugs have been marketed, and some of them became blockbuster drugs in market size. The patent expiration of the oldest biopharmaceutical drugs resulted in the development of biosimilar drugs. However the short serum half-life of biopharmaceutical drugs incurs a frequent injection to maintain a target clinical outcome in patients. The other major critical concern of biopharmaceutical drugs is immunogenicity producing anti-drug antibodies. These antibodies may reduce clinical efficacy by neutralizing biological activity, and may not only cause a severe allergic reaction but also other serious adverse reactions by blocking endogenous proteins. In order to improve pharmaceutical properties and reduce immunogenicity, the next generation biobetter drugs were achieved by glycoengineering technology, pegylation technology and protein engineering technology. Other biobetter drugs having optimized binding sites were also generated by in vitro display technology. Many of those biobetter drugs have been developed and/or are under development, and come into the clinical field in the near future.
引用
收藏
页码:900 / 911
页数:12
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