Gene/Protein
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Enzyme
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Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
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Target Concepts:
Gene/Protein
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Enzyme
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Query: UMLS:C0267964 (
PAA
)
2,561
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Inactivation and microbial regrowth of penicillin-,
ampicillin
-, cefalexin-, tetracycline-, chloramphenicol-, and rifampicin-resistant bacteria were studied to explore risks associated with selection and regrowth of antibiotic-resistant bacteria after
PAA
disinfection. The results showed that after exposure to 20 mg/L
PAA
for 10 min, inactivation of
ampicillin
-resistant bacteria reached 2.3-log, which was significantly higher than that of total heterotrophic bacteria with a decrease of 2.0-log. In contrast, inactivation of tetracycline- resistant bacteria was significantly less efficient, reaching only 1.1-log. Chloramphenicol-and tetracycline-resistant bacteria, as well as total heterotrophic bacteria regrew more than 10 fold compared to those in the untreated wastewater sample with 22 h stilling culture after exposure to 2 or 5 mg/L
PAA
as for 10 min. Selection and potential regrowth of tetracycline-and chloramphenicol-resistant bacteria are potential risks when utilizing
PAA
disinfection, which may induce the spread of specific antibiotic-resistant bacteria in reclaimed water.
...
PMID:Inactivation and regrowth of antibiotic-resistant bacteria by PAA disinfection in the secondary effluent of a municipal wastewater treatment plant. 2421 83
These studies show covalent attachment of multilayers (CAM) to chemically alter surfaces to achieve pH switchable antimicrobial and anticoagulant properties. Polyethylene (PE), poly(tetrafluoroethylene) (PTFE), and silicon (Si) surfaces were functionalized by tethering pH-responsive "switching" polyelectrolytes consisting of poly(2-vinyl pyridine) (P2VP) and poly(acrylic acid) (
PAA
) terminated with NH
2
and COOH groups, respectively. At pH < 2.3, the P2VP segments are protonated and expended, but at pH > 5.5, they collapse while the
PAA
segments are expanded. The presence of terminal NH
2
or COOH moieties on P2VP and
PAA
, respectively, facilitated the opportunity for covalently bonding
ampicillin
(
AMP
) and heparin (HEP) to both polyelectrolyte chains. Such surfaces, when exposed to S. aureus, inhibit the growth of microbial films (
AMP
) as well as anticoagulant properties (HEP). Comparison of "dynamic" pH dependent surfaces developed in these studies with "static" surfaces terminated with (
AMP
) entities shows significant enhancement in the longevity of surface activity against microbial film formation.
...
PMID:Covalent attachment of multilayers (CAM): a platform for pH switchable antimicrobial and anticoagulant polymeric surfaces. 3248 89