31.大环内酯类抗生素——山东大学药理学英文课件

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1、Chapter 38 Macrolides, Lincomycins and Polymycins,大环内酯类药物,14元大环内酯类:红霉素、罗红霉素、克拉霉素、地红霉素 15元大环内酯类:阿奇霉素 16元大环内酯类:螺旋霉素、乙酰螺旋霉素、麦迪霉素、麦白霉素、罗他霉素、柱晶白霉素、交沙霉素、米欧卡霉素,Macrolides,First generation : 1950serythromycin Second generation:1970sclaithromycin azithromycin Third generation:,Common properties of Macrolides

2、,Antibacterial activity,First generation Most G+ organisms: pneumococci, streptococci, staphylococci , diphtheriae etc Part G- organisms:legionella(军团菌),bacillus pertussis(百日咳), brucella(布氏) etc Others: mycoplasma(支原体), chlamydia trachomatis(沙眼衣原体), rickettsia(立克次体), spirochete ,anaerobes etc. Secon

3、d generation More active on G- organisms,Mechanism of action,Target 50s ribosomal RNA Mechanism inhibition of translocation of mRNA,Mechanism of resistance,Production of inactivating enzymes Modification of the ribosomal binding site Active efflux system MLSR,Pharmokinetics,Absorption Erythromycin:

4、not stable at acid pH New macrolides: stable po Distribution Metabolism: Erythromycin&clarithromycin: in liver Excretion Erythromycin& azithromycin: bile Clarithromycin: kidney,Commomly used macrolides,Erythromycin,Antimicrobial activity Gram-positive organisms: pneumococci, streptococci, staphyloco

5、cci , diphtheriae etc Gram-negative organisms:legionella(军团菌),bacillus pertussis(百日咳), brucella(布氏) , meningococci, diplococcus gonorrhoeae etc Others: mycoplasma(支原体), chlamydia trachomatis(沙眼衣原体), rickettsia(立克次体), spirochete ,anaerobes etc.,Erythromycin,Clinical uses As penicillin substitute in p

6、enicillin-allergic or resistant patients with infections caused by staphylococci, streptococci and pneumococci Pertussis,diphtheriae Legionella and mycoplasma pneumonia H.p infection,Erythromycin,Adverse reactions Gastrointestinal effects Liver toxicity Cardiotoxicity,Erythromycin,Erythromycin lacto

7、bionate(乳糖酸红霉素) erythromycin estolate(无味红霉素) erythromycin stearate(硬脂酸红霉素) erythromycin ethylsuccinate(琥乙红霉素, 利君沙),New macrolides antibiotics,Advantage : Broader spectrum, higher activity Orally effective High blood concentration Longer t 1/2 Less toxicity Mainly used in respiratory tract infection,

8、Clarithromycin(甲红霉素,克拉霉素),Has the strongest activity on Gram-positive bacteria, legionella pneumophila, chlamydia pneumoniae and H.p Good pharmacokinetic property Low toxicity,Azithromycin (阿齐霉素,丽珠奇乐),Has the strongest activity against mycoplasma pneumoniae(肺炎支原体) More effective on Gram-negative bac

9、teria Well tolerated T1/2 :3548h once daily Mainly used in respitory tract infection,Roxithromycin (罗红霉素,严迪),1987 France The highest blood concentration F 72%85% Respiratory tract infection and soft tissue infection Low adverse effects,Lincomycin and Clindamycin,Antimicrobial activity Gram-positive

10、organisms Bacteroide fragilis and other anaerobes Mechanism Binding to 50s ribosome subunit and inhibiting protein synthesis Pharmacokinetics Absorbed well Penetrate well into most tissues including bone,Clindaycin,Clinical uses Severe anaerobic infection Acute or chronical suppurative osteomylitis

11、, arthritis caused by susceptive organisms especially Staphylococci aureus Adverse reactions Gastrointestinal effects: severe diarrhea and pseudomembranous enterocolitis caused by Clostridium difficile :vancomycin & metronidazole Other :Impaired liver function , neutropenia,Polypeptide antibiotics,V

12、ancomycin & Teicoplanin Polymyxins bactitracin,Vancomycin,Mechanism of action Inhibit cell wall synthesis Antimicrobial spectrum: Narrow spectrum, active only against gram-positive bacteria paticularly staphylococci Pharmacokinetics Poorly absorbed from intestinal tract, iv Excreted from glomerular

13、filtration 90%,Vancomycin,Clinical uses Infection caused by MRSA, MRSE and penicillin-resistant pneumococcus Treatment of antibiotic-associated enterocolitis caused by clostridium difficile po Adverse reaction Ototoxicity & nephrotoxicity Red-man syndrome,Teicoplanin,Similar to vancomycin in mechani

14、sm and antimicrobial spectrum Can be given im as well as iv Less adverse reactions,Polymyxins,Active only against gram-negative rods, particularly P.aeruginosa Mechanism:increase permeability of cell membrane Mainly used in P.aeruginosa infection when other drugs are resistant Toxicity: nephrotoxicity & neurotoxicity,Baciteracin,Active against gram-positive bacteria Inhibit cell wall formation No cross-resistance with other agents Topical use only because of nephrotoxicity,

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