article review on adalimumab production
Adalimumab is a recombinant
human monoclonal antibody that is used to treat a variety of inflammatory
diseases, such as rheumatoid arthritis, psoriasis, and Crohn's disease. It is
produced using recombinant DNA technology in Chinese hamster ovary (CHO) cells.
A research article
"Development of a high-titer, high-density fed-batch process for the
production of adalimumab in CHO cells" by Chen et al. (2018) aimed to
improve the production of adalimumab by developing a high-titer and
high-density fed-batch process. The study used a CHO cell line that had been
modified to express the adalimumab gene. The cells were grown in a culture
medium containing glucose, amino acids, and a proprietary feed supplement, and
the culture conditions were optimized to achieve high yields of the protein.
The results of the study
showed that a high yield of adalimumab (over 2g/L) was achieved using the
fed-batch cultivation system. The study also found that the specific
productivity of the cells was highest during the late exponential phase of the
culture. The study also demonstrated that the quality of the protein was
similar to that of the clinically used product, with a high degree of purity,
stability, and bioactivity.
In conclusion, the study by
Chen et al. (2018) provides valuable insights into the production of adalimumab
using CHO cells. The findings demonstrate that high yields of the protein can
be achieved using a high-titer, high-density fed-batch cultivation system, with
the highest specific productivity during the late exponential phase of the
culture. The study also shows that the protein produced has a similar quality
to clinically used product, which is important for the efficacy of the drug.
As a review, the study is
well-conducted, with a clear research objective, methodology, and results. The
results are well-interpreted and the conclusion is well-supported by the data.
The study provides a good example of how to optimize the culture conditions and
the feeding strategy to achieve high yields of a recombinant protein.
Additionally, the study is well-referenced and provides a good background
information, and more research is needed to establish the scalability of the
process and to understand the cost-benefit of the process.
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