Science, asked by kishorilal6464, 1 month ago

explain the discovery of penicillin​

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Answered by Feirxefett
6

Answer:

Alexander Fleming's Discovery

After isolating the mold and identifying it as belonging to the Penicillium genus, Fleming obtained an extract from the mold, naming its active agent penicillin. He determined that penicillin had an antibacterial effect on staphylococci and other gram-positive pathogens.

Answered by sabitrinahak1980
1

Answer:

After just over 75 years of penicillin’s clinical use, the world can see that its impact was immediate and profound. In 1928, a chance event in Alexander Fleming’s London laboratory changed the course of medicine. However, the purification and first clinical use of penicillin would take more than a decade. Unprecedented United States/Great Britain cooperation to produce penicillin was incredibly successful by 1943. This success overshadowed efforts to produce penicillin during World War II in Europe, particularly in the Netherlands. Information about these efforts, available only in the last 10–15 years, provides new insights into the story of the first antibiotic. Researchers in the Netherlands produced penicillin using their own production methods and marketed it in 1946, which eventually increased the penicillin supply and decreased the price. The unusual serendipity involved in the discovery of penicillin demonstrates the difficulties in finding new antibiotics and should remind health professionals to expertly manage these extraordinary medicines.

Keywords: penicillin, discovery, antimicrobial drugs, antibiotics, history of medicine

According to British hematologist and biographer Gwyn Macfarlane, the discovery of penicillin was “a series of chance events of almost unbelievable improbability” (1). After just over 75 years of clinical use, it is clear that penicillin’s initial impact was immediate and profound. Its detection completely changed the process of drug discovery, its large-scale production transformed the pharmaceutical industry, and its clinical use changed forever the therapy for infectious diseases. The success of penicillin production in Great Britain and the United States overshadowed the serendipity of its production and the efforts of other nations to produce it. Information on penicillin production in Europe during World War II, available only in the last 10–15 years, provides new insights into penicillin’s story.

Dawn of Chemotherapy and the “Magic Bullet”

At the beginning of the 20th century, Paul Ehrlich pioneered the search for a chemical that would kill a microorganism and leave the host unaltered—the “magic bullet.” Ehrlich also coined the term chemotherapy: “There must be planned chemical synthesis: proceeding from a chemical substance with recognizable activity, making derivatives from it, and then trying each to discover the degree of its activity and effectiveness. This we call chemotherapy” (2). After extensive testing, he found a drug with activity against the bacterium Treponema pallidum, which causes syphilis. The introduction of this drug, arsphenamine (Salvarsan), and its chemical derivative neoarsphenamine (Neosalvarsan) in 1910 ushered in a complete transformation of syphilis therapy and the concept of chemotherapy. Unfortunately, despite exhaustive searches, the promise of more magic bullets for microbial therapy remained elusive. For 20 years, Salvarsan and Neosalvarsan were the only chemotherapy for bacterial infections.

Alexander Fleming’s Discovery

A chance event in a London laboratory in 1928 changed the course of medicine. Alexander Fleming, a bacteriologist at St. Mary’s Hospital, had returned from a vacation when, while talking to a colleague, he noticed a zone around an invading fungus on an agar plate in which the bacteria did not grow. After isolating the mold and identifying it as belonging to the Penicilliumgenus, Fleming obtained an extract from the mold, naming its active agent penicillin. He determined that penicillin had an antibacterial effect on staphylococci and other gram-positive pathogens.

Fleming published his findings in 1929 (3). However, his efforts to purify the unstable compound from the extract proved beyond

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