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Timeline

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Pharmaceutical engineering

Planned Additions

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  1. A section describing the history of the industry and the formation of the ISPE
  2. A big picture view of the overall process, from research to development to manufacturing


Activity: Add a citation

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Steady-state conduction
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This sub-section has no citations and some statements made without stating assumptions. My source, Fundamentals of Heat and Mass Transfer,[1] describes the phenomena of steady-state conduction. Specifically, this section describes how the temperature distribution in a rod with two different end temperatures varies linearly with space. This temperature distribution will only be linear in the case of no internal heat generation. I edited the sentence to add this condition, then added the citation.

Draft: History section for pharmaceutical engineering

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Humans have a long history of using derivatives of natural resources, such as plants, as medication. However, it was not until the late 19th century when the technological advancements of chemical companies were combined with medical research that scientists began to manipulate and engineer new medications, drug delivery techniques, and methods of mass production.[2]

Synthesizing new medications

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One of the first prominent examples of an engineered, synthetic medication was made by Paul Erlich. Erlich had found that Atoxyl, an arsenic-containing compound which is harmful to humans, was very effective at killing Treponema pallidum, the bacteria which causes Syphilis. He hypothesized that if the structure of Atoxyl was altered, a “magic bullet” could potentially be identified which would kill the parasitic bacteria without having any adverse effects on human health.[3] He developed many compounds stemming from the chemical structure of Atoxyl and eventually identified one compound which was the most effective against Syphilis while being the least harmful to humans, which became known as Salvarsan. Salvarsan was widely used to treat Syphilis within years of its discovery.[4]   

Beginning of mass production

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In 1928, Alexander Fleming discovered a mold named Penicillium chrysogenum which prevented many types of bacteria from growing. Scientists identified the potential of this mold to provide treatment in humans against bacteria which cause infections. During World War II, the United Kingdom and the United States worked together to find a method of mass producing Penicillin[5], a derivative of the Penicillium mold, which had the potential to save many lives during the war since it could treat infections common in injured soldiers. Although Penicillin could be isolated from the mold in a laboratory setting, there was no known way to obtain the amount of medication needed to treat the quantity of people who needed it. Scientists with major chemical companies such as Pfizer were able to develop a deep-fermentation process which could produce a high yield of penicillin. In 1944, Pfizer opened the first penicillin factory, and its products were exported to aid the war efforts overseas.[6]

Controlled drug release

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Tablets for oral consumption of medication have been utilized since approximately 1500 B.C.[7], however for a long time the only method of drug release was immediate dissolution, meaning all of the medication is released in the body at once.[8] In the 1950s, sustained release technology was developed. Through mechanisms such as osmosis and diffusion, pills were designed that could release the medication over a 12-hour to 24-hour period. Smith, Kline & French developed one of the first major successful sustained release technologies. Their formulation consisted of a collection of small tablets taken at the same time, with varying amounts of wax coating that allowed some tablets to dissolve in the body faster than others.[9] The result was a continuous release of the drug as it travelled through the intestinal tract. Although modern day research focuses on extending the controlled release timescale to the order of months, once-a-day and twice-a-day pills are still the most widely utilized controlled drug release method.[8]

Formation of the ISPE

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In 1980, the International Society for Pharmaceutical Engineering was formed to support and guide professionals in the pharmaceutical industry through all parts of the process of bringing new medications to the market. The ISPE writes standards and guidelines for individuals and companies to use and to model their practices after. The ISPE also hosts training sessions and conferences for professionals to attend, learn, and collaborate with others in the field.[10]

*** Note: I plan to delete the sentence originally in the article about the ISPE, as it doesn't offer any more information than 'it exists'. My section on the ISPE will give a better idea of what the ISPE is, so the other sentence is no longer necessary in my opinion.

Figures to add to Pharmaceutical engineering

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Equipment for deep-fermentation of penicillin
  • Penicillin bioreactor
  • Image to accompany tablet formation section




Draft: See Also section for Pharmaceutical engineering

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  1. ^ Fundamentals of heat and mass transfer. Bergman, T. L., Incropera, Frank P. (7th ed. ed.). Hoboken, NJ: Wiley. 2011. ISBN 9780470501979. OCLC 713621645. {{cite book}}: |edition= has extra text (help)CS1 maint: others (link)
  2. ^ "Top Pharmaceuticals: Introduction: EMERGENCE OF PHARMACEUTICAL SCIENCE AND INDUSTRY: 1870-1930". pubs.acs.org. Retrieved 2019-02-14.
  3. ^ Williams, KJ (2009-08-01). "The introduction of 'chemotherapy' using arsphenamine – the first magic bullet". Journal of the Royal Society of Medicine. 102 (8): 343–348. doi:10.1258/jrsm.2009.09k036. ISSN 0141-0768. PMC 2726818. PMID 19679737.{{cite journal}}: CS1 maint: PMC format (link)
  4. ^ "Chemical & Engineering News: Top Pharmaceuticals: Salvarsan". pubs.acs.org. Retrieved 2019-02-14.
  5. ^ Quinn, Roswell (2013-3). "Rethinking Antibiotic Research and Development: World War II and the Penicillin Collaborative". American Journal of Public Health. 103 (3): 426–434. doi:10.2105/AJPH.2012.300693. ISSN 0090-0036. PMC 3673487. PMID 22698031. {{cite journal}}: Check date values in: |date= (help)CS1 maint: PMC format (link)
  6. ^ "Penicillin Production through Deep-tank Fermentation - National Historic Chemical Landmark". American Chemical Society. Retrieved 2019-02-14.
  7. ^ MESTEL, ROSIE (2002-03-25). "The Colorful History of Pills Can Fill Many a Tablet". Los Angeles Times. ISSN 0458-3035. Retrieved 2019-03-19.
  8. ^ a b Yun, Yeon Hee; Lee, Byung Kook; Park, Kinam (2015-12-10). "Controlled Drug Delivery: Historical perspective for the next generation". Journal of controlled release : official journal of the Controlled Release Society. 219: 2–7. doi:10.1016/j.jconrel.2015.10.005. ISSN 0168-3659. PMC PMCPMC4656096. PMID 26456749. {{cite journal}}: Check |pmc= value (help)
  9. ^ Oral controlled release formulation design and drug delivery : theory to practice. Hoboken, N.J.: Wiley. 2013. ISBN 9781118060322. OCLC 898985497.
  10. ^ "About ISPE". ISPE | International Society for Pharmaceutical Engineering. Retrieved 2019-02-15.