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Tetracycline case

In the so-called tetracycline case (2), there was evidence that in the preparation of aureomycin broth by the fermentation of S, aureo-faciens, some small percentage of tetracycline was coproduced. Aureomycin was known and produced by fermentation substantially before the discovery of tetracycline. The argument was raised by the patent examiner when the tetracycline application was in the Patent Office that tetracycline must be produced inherently in the fermentation in the production of aureomycin. The applicant was able to show, however, that the amount of tetracycline produced in the fermentation broth in aureomycin production was so small that it was of inconsequential value to mankind as an antibiotic. In fact, most methods of analysis did... [Pg.111]

ERGOT DERIVATIVES TETRACYCLINES Cases of ergotism with tetracyclines and ergotamine Uncertain Avoid co-administration. If absolutely necessary, advise patients to discontinue treatment immediately if numbness and tingling of the extremities are felt... [Pg.228]

The iacreased chemical stabiUty of the 6-deoxytetracyclines allows chemical modification with retention of biological activity electrophilic substitutions have been carried out at C-7 and C-9 under strongly acidic conditions (46—53). Reactions of 6-deoxy-6-demethyltetracycline [808-26-4] (16), C21H22N2O7, with electrophiles, such as nitrate ion (49), bromomium ion (46,47) (from N-bromosuccinimide), or N-hydroxymethylphthalimide (53), yielded 7-substituted tetracyclines. In the case of the nitration reaction, both the 7- and 9-nitro isomers (17, X = NO2, Y = H) and (17, X = H, Y = NO2) were obtained. [Pg.179]

Efforts have been made to correlate electronic stmcture and biological activity in the tetracycline series (60,61). In both cases, the predicted activities are of the same order as observed in vitro with some exceptions. The most serious drawback to these calculations is the lack of carryover to in vivo antibacterial activity. Attempts have also been made (62) to correlate partition coefficients and antibacterial activity. The stereochemical requirements are somewhat better defined. Thus 4-epitetracycline and 5a-epitetracycline [65517-29-5] C22H24N20g, are inactive (63). The 6-epi compound [19369-52-9] is about one-half as active as the 6a (or natural) configuration. [Pg.180]

Tetracyclines are used as alternative dnigs in a variety of circumstances when the patient is unable to take the dnig of choice, eg, in patients allergic to penicillin (88,89). Tetracyclines are widely known to cause staining of teeth (and are therefore contra-indicated in children developing permanent teeth), photosensitivity, and, in the case of minocycline, vestibular toxicity. Details of these adverse effects and others associated with administration of tetracyclines have been comprehensively reviewed (96—101). [Pg.182]

In some cases, catechins can also act in synergistic mode when used in association with currently used antibiotic molecules (Table 2). EGCG exhibited synergy with /3-lactams. Sudano Roccaro et al. [73] found that this compound is able to reverse tetracycline resistance in Staphylococcus epidermidis and S. aureus isolates. This synergistic interaction has been explained by inhibition of tetracycline efflux pump activity in microbial cells resulting in an... [Pg.250]

Reduced absorption due to complex formation or other interactions between drugs and intestinal components leading to poor absorption has been described in a few cases. One example is the precipitation of cationic drugs as very poorly-soluble salts with bile acids, which has been reported for several compounds [62], Another well-known example is the complex formation between tetracycline together with calcium due to chelation after administration of the drug together... [Pg.513]

Trimethoprim-sulfamethoxazole (or trimethoprim alone) is a second-line oral agent that may be used for patients who do not tolerate tetracyclines and erythromycin or in cases of resistance to these antibiotics. The adult dose is usually 800 mg sulfamethoxazole and 160 mg trimethoprim twice daily. [Pg.198]

Case reports have shown a reduction in EE levels when CHCs are taken with tetracyclines and penicillin derivatives. The Council on Scientific... [Pg.349]

Macrolide antibiotics (clarithromycin, dehydroerythromycin, etc.) and sulfonamides (sulfamethoxazole, sulfadimethoxine, sulfamethazine, and sulfathi-azole) are the most prevalent antibiotics found in the environment with levels around a few micrograms per liter, whereas fluoroquinolones, tetracyclines, and penicillins have been detected in fewer cases and usually at low concentrations (nanograms per liter) [3,20,23,72]. This result is not surprising, since penicillins are easily hydrolyzed and tetracyclines readily precipitate with cations such as calcium and are accumulated in sewage sludge or sediments. Several reviews have reported the environmental occurrence of different antibiotics in aquatic and soil compartments. Some of these data are detailed in Table 1. [Pg.199]

We have found only one attempt to use immunoassays to detect sulfonamides in environmental samples. As in the case of penicillins and tetracyclines and also for fluoroquinolones (see below), Campagnolo et al. [84] measured sulfonamides in water samples proximal to a farm in Iowa using a commercial Charm II RIA test, accomplishing a LOD of 5 pg L 1 for sulfamethazine. [Pg.215]

Tetracycline 500 mg every six hours or doxycycline 100 mg every twelve hours for five to seven days will shorten the duration of illness, and fever usually disappears within one to two days after treatment is begun. Ciprofloxacin and other quinolones are active in vitro and should be considered for victims unable to take tetracycline or doxycycline. Successful treatment of Q fever endocarditis is much more difficult. Tetracycline or doxycycline given in combination with trimethoprim-sulfamethoxazole (TMP-SMX) or rifampin for twelve months or longer has been successful in some cases. However, valve replacement is often required to achieve a cure. [Pg.160]

Because human cases of glanders are rare, there is limited information shout antibiotic treatment of the organism in humans. Sulfadiazine has been found to be an effective in experimental animals and in humans SutfMderiente/fer is usually sensitive to tetracyclines, ciproflacacin, streptomycin, novobiocin, gentamicin, imipenem, ceftazidime, and the sulfonamides Resistance to chloramphenicol has been reported. [Pg.385]

Treatment — Various antibiotics are useful in treating Coxiella infections. They include tetracycline, doxycycline, and erythromycin. In cases of endocarditis, treatments with doxycycline combined with rifampin, and trimethoprim-sulfamethoxazole combined with doxycycline or tetracycline for 12 months or longer have been successful.3... [Pg.99]

Once the recombinant vectors have been produced, they are used to transform host cells. In the example of the plasmid pBR322, the host cells are bacteria. Once transformed, the bacteria are plated on selective media so that bacteria transformed with a recombinant plasmid can be easily identified. In the case of plasmid pBR322 shown in Figure 1-6-3, bacteria with recombinant plasmids would be resistant to ampicillin but sensitive to tetracycline. [Pg.84]

Several classes of antibiotics, e.g., tetracyclines [86], fluoroquinolones [87, 88], and p-lactams [89] were observed to react with chemical oxidants such as chlorine dioxide (CIO2) and free chlorine. Oxidation with CIO2 yields hydroxylated and oxygenated products in the case of tetracyclines, and leads to dealkylation, hydroxylation, and intramolecular ring closure at the piperazine moiety of the fluoroquinolones [86, 88]. [Pg.113]

Administration of 100 mg doxycycline, in the absence of foods, led to almost complete absorption from the gut and a peak blood level of 1-8 Mg/ml two hours after ingestion. Three times this dose was required.to produce a similar blood level in four hours in the case of 300 mg demethylchlortetracycline. The plasma half-life (after single dose) was 15 hours in the case of doxycycline and 12 hours for demethylchlortetracycline. This means that the half-life of doxycycline is seven hours longer than that of tetracycline. [Pg.9]

Since patients can rarely be relied upon to take (or be given) medication after fasting, and since itis common experience that doses are omitted more or less frequently the properties of doxycycline make it appear a promising successor to the first generation tetracyclines. This is even more likely since the antibacterial spectrum and activity is at least equal to that of tetracycline, and in the case of certain tetracycline-resistant bacteria doxycycline has (of all derivatives tested) shown the highest activity [35, 41]. [Pg.11]

A senior British government veterinarian stated in 1962 (3)> When penicillin was first used in treating mastitis only 2% of the strains of staphylococci recovered from cases of mastitis were resistant to penicillin. Today the figure is over 70%. Between 1958 and 1961, resistance to penicillin (PEN) increased from 62.0% to 70.6%. Resistance to streptomycin (STR), tetracycline and chloramphenicol also increased (. Antibiotic resistance increased for isolates of both mastitis staphylococci and streptococci in Canada between I960 and 1967 (5). In Belgium (6), Staphylococcus aureus strains isolated from cases of bovine mastitis showed increase in PEN resistance from 38% in 1971 to 78% in 1974> but then no further increase to 1980. The resistance situation was reported to remain stable in the Federal Republic of Germany between 1962 and 1975 (7), as also in Australia between 1974 and 1979 (8 ) and Denmark, at a very low level, for the period 1963 to 1978 (9). [Pg.24]

Numerous cases of the use of antibiotics(especially cycloheximide, ohyamycin, streptomycin, tetracyclines, penicillin, griseofulvin, and polymyxin) against several bacterial and fungal diseases are now known(33-35). In the United States of America, Merck sells preparations of streptomycin and Upjohn sells that of cycloheximide for the control of the diseases of ornamental plants(R.Burg,... [Pg.51]


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See also in sourсe #XX -- [ Pg.104 ]




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