Will the Drugs of the Future Be Small Molecules or Biological Drugs?

被引:1
|
作者
Radl, Stanislav [1 ]
Dammer, Ondrej [1 ]
Ridvan, Ludek [1 ]
机构
[1] Zentiva KS, U Kabelovny 130, Prague 10237, Czech Republic
来源
CHEMICKE LISTY | 2022年 / 116卷 / 08期
关键词
small molecules; biologics; biosimilars; poly-morphs; solvates; cocrystals; amorphous solid dispersions; lipidic formulations; ORAL DELIVERY; INCREASING BIOAVAILABILITY; MONOCLONAL-ANTIBODIES; FORMULATIONS; DISPERSIONS; SOLUBILITY; ACETATE;
D O I
10.54779/chl20220471
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
After the approval of the first therapeutic monoclonal antibodies and their successful introduction into therapy, a great future was expected for this class of drugs. This assumption has been fulfilled to a limited extent only, es-pecially in the treatment of oncological problems, some autoimmune diseases and in the treatment of some rare diseases. On the other hand, a considerable progress has been made in the fields of oncology and autoimmune dis-eases by discovering protein kinases, and these small mol-ecule drugs represent alternatives in the treatment of a range of such diseases. In this article, we have tried to shed light mainly on the role of small molecules in thera-py, including problems connected with the development of this class of drugs. For many of them, their physico- chemical properties prevent using traditional formulation techniques and modern technologies must be applied. This paper summarizes the most commonly used approaches for increasing bioavailability, including both the prodrug ap-proach and the use of various solid forms of the active ingredient in specific formulations available on the market. The article also provides examples of practical use of amorphous solid dispersions and modern trends, including the development of various types of lipid formulations.
引用
收藏
页码:471 / 480
页数:10
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