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Penicillin

About: Penicillin is a research topic. Over the lifetime, 17916 publications have been published within this topic receiving 368480 citations. The topic is also known as: penicillin antibiotic & PCN.


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Journal ArticleDOI
TL;DR: Adverse reactions to penicillin occur in 1 to 8 per cent of patients treated, and the different reaction rates are probably related to numerous factors, including the difficulty in attributing reactions specifically to Penicillin, particularly when several drugs are being administered.
Abstract: THE remarkable lack of pharmacologic toxicity of penicillin is now well established, but penicillin hypersensitivity reactions have become a serious problem. A projection of statistics from some surveys estimates that 100 to 300 fatalities occur annually in the United States from reactions to penicillin,1 and an estimated 2,500,000 people in the United States are allergic to this widely used antibiotic.2 Adverse reactions to penicillin occur in 1 to 8 per cent of patients treated.3 The different reaction rates are probably related to numerous factors, including the difficulty in attributing reactions specifically to penicillin, particularly when several drugs are being administered . . .

290 citations

Journal ArticleDOI
TL;DR: Penicillin has been shown to be an effective antiseptic for application to, or injection into, areas infected with penicillin-sensitive microbes, e.g. B. influenzae as mentioned in this paper.
Abstract: 1. A certain type of penicillium produces in culture a powerful antibacterial substance. The antibacterial power of the culture reaches its maximum in about 7 days at 20o C. and after 10 days diminishes until it has almost disappeared in 4 weeks. 2. The best medium found for the production of the antibacterial substance has been ordinary nutrient broth. 3. The active agent is readily filterable and the name "penicillin" has been given to filtrates of broth cultures of the mould. 4. Penicillin loses most of its power after 10 to 14 days at room temperature but can be preserved longer by neutralization. 5. The active agent is not destroyed by boiling for a few minutes but in alkaline solution boiling for 1 hour markedly reduces the power. Autoclaving for 20 minutes at 115o C. practically destroys it. It is soluble in alcohol but insoluble in ether or chloroform. 6. The action is very marked on the pyogenic cocci and the diphtheria group of bacilli. Many bacteria are quite insensitive, e.g. the coli-typhoid group, the influenza-bacillus group, and the enterococcus. 7. Penicillin is non-toxic to animals in enormous doses and is non-irritant. It doses not interfere with leucocytic function to a greater degree than does ordinary broth. 8. It is suggested that it may be an efficient antiseptic for application to, or injection into, areas infected with penicillin-sensitive microbes. 9. The use of penicillin on culture plates renders obvious many bacterial inhibitions which are not very evident in ordinary cultures. 10. Its value as an aid to the isolation of B. influenzae has been demonstrated.

288 citations

Journal Article
TL;DR: Detailed characterization of clindamycin uptake confirmed that the drug is accumulated by an active transport system, and should provide information useful in establishing guidelines for optimal antibiotic usage.

287 citations

Journal ArticleDOI
TL;DR: Ten strains were sensitive to the Gram-positive spectrum antibiotics erythromycin and novobiocin, the broad-spectrum antibiotics rifampicin, spectinomycin, tetracycline and chloramphenicol and the beta-lactam antibiotics penicillin, ampicillin and cephalothin.

287 citations

Journal ArticleDOI
TL;DR: The position that testing with PPL, PA, and Pen G is a rapid, safe, and effective method for identifying patients atrisk, or not at risk, for allergic reactions to penicillin is supported.
Abstract: Skin testing for penicillin allergy with penicillin G (Pen G), penicilloic acid (PA), and penicilloyl poly-L-lysine (PPL) was performed on 740 subjects, and the results were assessed from epidemiologic and immunologic perspectives. Approximately 95% of these patients had histories of apparent allergic reactions to beta-lactam antibiotics, and 63% were skin-test positive. The prevalence of positive skin tests was related to the time that had elapsed between clinical reactions and skin testing. Ninety-three percent were skin-test positive 7 to 12 mo after reactions, and 22% were positive 10 yr or more after reactions. Patients under 30 yr of age had a prevalence of positive skin tests 1.7-fold higher than older patients. Testing with PPL, PA, and Pen G detected 76.3%, 55.3%, and 57.1% of the positive patients, respectively. Omission of PPL, PA, or Pen G would have led to a failure to detect 25.6%, 7.2%, and 6.2% of the positive patients, respectively. Subjects with skin tests positive to penicillin often reacted to skin tests with other beta-lactam antibiotics; 73% (41 of 56) reacted to ampicillin and 51% (38 of 74) reacted to cephalothin. No serious allergic reactions were provoked by testing. None of the 83 skin test--negative patients treated with beta-lactam antibiotics immediately after testing experienced acute allergic reactions. Two patients developed mild urticaria beginning 3 and 5 days into therapy. One skin test--negative patient experienced urticaria 3 hr after receiving oral penicillin 6 mo after skin testing. This patient's skin-test status immediately before therapy was unknown. These results support the position that testing with PPL, PA, and Pen G is a rapid, safe, and effective method for identifying patients at risk, or not at risk, for allergic reactions to penicillin.

285 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023459
2022907
2021249
2020269
2019221
2018192