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Crystalline monoclonal antibodies for subcutaneous delivery
- Source :
- Proceedings of the National Academy of Sciences of the United States of America. 100(12)
- Publication Year :
- 2003
-
Abstract
- Therapeutic applications for mAbs have increased dramatically in recent years, but the large quantities required for clinical efficacy have limited the options that might be used for administration and thus have placed certain limitations on the use of these agents. We present an approach that allows for s.c. delivery of a small volume of a highly concentrated form of mAbs. Batch crystallization of three Ab-based therapeutics, rituximab, trastuzumab, and infliximab, provided products in high yield, with no detectable alteration to these proteins and with full retention of their biological activity in vitro . Administration s.c. of a crystalline preparation resulted in a remarkably long pharmacokinetic serum profile and a dose-dependent inhibition of tumor growth in nude mice bearing BT-474 xenografts (human breast cancer cells) in vivo . Overall, this approach of generating high-concentration, low-viscosity crystalline preparations of therapeutic Abs should lead to improved ease of administration and patient compliance, thus providing new opportunities for the biotechnology industry.
- Subjects :
- Male
medicine.drug_class
Injections, Subcutaneous
Transplantation, Heterologous
Mice, Nude
Antineoplastic Agents
Breast Neoplasms
Pharmacology
Monoclonal antibody
Antibodies, Monoclonal, Humanized
Antibodies, Monoclonal, Murine-Derived
Mice
In vivo
Trastuzumab
medicine
Animals
Humans
Mice, Inbred BALB C
Multidisciplinary
Chemistry
Antibodies, Monoclonal
Biological Sciences
In vitro
Infliximab
Rats
Transplantation
Connective Tissue
Monoclonal
Cancer cell
Rituximab
Female
Crystallization
Neoplasm Transplantation
medicine.drug
Subjects
Details
- ISSN :
- 00278424
- Volume :
- 100
- Issue :
- 12
- Database :
- OpenAIRE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Accession number :
- edsair.doi.dedup.....83d01aae1936113b3742b0adcff48536