Drugs technology

Lebedeva I., Stein C.A., Annu. Rev. Pharmacol. Toxicol. 2001, 43, 403-419. Antisense Drug Technology - Principles, Strategies and Applications, Crooke S.T. (Ed.). M. Decker, 2001. 

Phillips, M. 2000. Antisense Technology. Methods in Enzymology, volume 313. Academic Press. Crooke, S. (Ed.) 2001. Antisense Drug Technology. Marcel Dekker. 

Psychedelics are the newest addition to drug technology in our culture. While the use of many of these substances in their plant form is very old, their use in our culture is... 

FIGURE 17.4 Particle size distribution of a steroid processed in a wet ball mill as measured by light scattering. (Data generated by NanoSystems, Elan Drug Technologies, a member of the Elan Corporation, pic.)... 

Source Data generated by NanoSystems, Elan Drug Technologies, a memberofthe Elan Corporation, pic. 

Levin AA, Yu RZ, Geary RS. Basic Principles of the Pharmacokinetics Of antisense Oligonucleotide drugs. In Crooke ST, ed. Antisense Drug Technology. New York Dekker, 2007. 

Koch T, Oerum, H. Locked nucleic acids. In Antisense Drug Technologies Principals, Strategies, and Applications. 2nd edition. 

Rao, A.V. Rajan, J.V. Transfer of drug technology from laboratory to industry. Eastern Pharmacist (India) 1985, 28, 63-65. 

Vollmer J, Krieg A. Mechanisms and therapeutic applications of immune modulatory oligodeoxynucleotide and oligoribonucleotide ligands for toll-like receptors. In Crooke ST, ed., Antisense Drug Technology, Boca Raton Taylor Francis 2007 747-772. 

M. A. Macrisand P. M. Glazer, Antisense Drug Technology Principles, Strategies, and Applications, Marcel Dekker, New York, 2001, pp. 859-886. 

Bhanot, S. (2008) Developing antisense chugs for metabolic diseases a novel therapeutic approach. In Crooke, S.T. (ed.), Antisense Drug Technology, 2nd edition. CRC Press LLC, Boca Raton, FL, pp. 641 663. 

In its broadest definition, so as to capture all the activities for its execution, the scope of bulk drug technology transfer... 

The internal diameter of CD is larger than that of /0-CD, and 2f-CD yields complexes more easily with spironolactone. During 1 hour, the total pharmacon dissolves from the physical mix /Figure l b/ this quantity is 25 times more than that from pure spironolactone. The preparation of a physical mix is the simplest and cheapest drug technological operation. 

Medicines and Drugs Technology Institute, Oswaldo Cruz Foundation, Rio de Janeiro, RJ, Brazil " Laboratory of Enzyme Technology, Biochemistry Department, Chemistry Institute, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro, RJ, Brazil... 

Medicines and Drugs Technology Institute Oswaldo Cruz Foundation Rio de Janeiro, RJ Brazil... 

Crooke ST (ed) (2001) Antisense drug technology principles, strategies, and applications. Marcel Dekker, New Yrak... 

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