<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>clavulinic acid Archives - Online Biology Notes</title>
	<atom:link href="https://www.onlinebiologynotes.com/tag/clavulinic-acid/feed/" rel="self" type="application/rss+xml" />
	<link></link>
	<description>A Complete notes for Students</description>
	<lastBuildDate>Tue, 18 Dec 2018 17:26:53 +0000</lastBuildDate>
	<language>en-US</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	
	<item>
		<title>Beta-lactam antibiotics: Penicillin, Cephalosporin, Monobactam, Carbapenems and Clavulanic acid</title>
		<link>https://www.onlinebiologynotes.com/beta-lactam-antibiotics-penicillin-cephalosporin-monobactam-carbapenems-and-clavulanic-acid/</link>
		
		<dc:creator><![CDATA[Gaurab Karki]]></dc:creator>
		<pubDate>Sun, 08 Apr 2018 03:11:30 +0000</pubDate>
				<category><![CDATA[Pharmaceutical Microbiology]]></category>
		<category><![CDATA[antimicrobial activity of beta lactam antibiotics]]></category>
		<category><![CDATA[beta-lactam antibiotics]]></category>
		<category><![CDATA[carbapenems]]></category>
		<category><![CDATA[chcephalosporin]]></category>
		<category><![CDATA[clavulinic acid]]></category>
		<category><![CDATA[maonbactam]]></category>
		<category><![CDATA[mode of action of beta lactam antibiotics]]></category>
		<category><![CDATA[PBP]]></category>
		<category><![CDATA[penicillin]]></category>
		<category><![CDATA[protein binding protein]]></category>
		<guid isPermaLink="false">http://www.onlinebiologynotes.com/?p=1324</guid>

					<description><![CDATA[<p>Beta-lactam antibiotics: Penicillin, Cephalosporin, Monobactam, Carbapenems and Clavulanic acid β-lactam antibiotics have common b-lactam ring in their structure. Different b lactam antibiotics differ in their <a class="mh-excerpt-more" href="https://www.onlinebiologynotes.com/beta-lactam-antibiotics-penicillin-cephalosporin-monobactam-carbapenems-and-clavulanic-acid/" title="Beta-lactam antibiotics: Penicillin, Cephalosporin, Monobactam, Carbapenems and Clavulanic acid">[...]</a></p>
<p>The post <a href="https://www.onlinebiologynotes.com/beta-lactam-antibiotics-penicillin-cephalosporin-monobactam-carbapenems-and-clavulanic-acid/">Beta-lactam antibiotics: Penicillin, Cephalosporin, Monobactam, Carbapenems and Clavulanic acid</a> appeared first on <a href="https://www.onlinebiologynotes.com">Online Biology Notes</a>.</p>
]]></description>
										<content:encoded><![CDATA[<h1>Beta-lactam antibiotics: Penicillin, Cephalosporin, Monobactam, Carbapenems and Clavulanic acid</h1>
<ul>
<li>β-lactam antibiotics have common b-lactam ring in their structure. Different b lactam antibiotics differ in their side chain.</li>
</ul>
<p>There are several types of B-lactam antibiotics which are potentially important.</p>
<p><img fetchpriority="high" decoding="async" class="aligncenter size-full wp-image-1328" src="http://www.onlinebiologynotes.com/wp-content/uploads/2018/04/list-of-beta-lactam-antibiotics.jpg" alt="" width="693" height="446" srcset="https://www.onlinebiologynotes.com/wp-content/uploads/2018/04/list-of-beta-lactam-antibiotics.jpg 693w, https://www.onlinebiologynotes.com/wp-content/uploads/2018/04/list-of-beta-lactam-antibiotics-300x193.jpg 300w" sizes="(max-width: 693px) 100vw, 693px" /></p>
<p>Some of them are:</p>
<ol>
<li><a href="http://www.onlinebiologynotes.com/penicillin-classification-mode-of-action-and-penicillin-resistance/"><strong>Penicillin-</strong></a> penicillin G, methicillin, amphicillin, amoxicillin, carbenicillin, piperacillin, penicillin V</li>
<li><a href="http://www.onlinebiologynotes.com/cephalosporin-structure-classification-clinical-use-and-mode-of-action/"><strong>Cephalosporin</strong></a></li>
<li><strong>Monobactam</strong></li>
<li><strong>Carbapenems</strong></li>
<li><strong>Clavamas-clavulanic acid</strong></li>
</ol>
<h2>1. <a href="http://www.onlinebiologynotes.com/penicillin-classification-mode-of-action-and-penicillin-resistance/">Penicillin</a></h2>
<h2>2. <a href="http://www.onlinebiologynotes.com/cephalosporin-structure-classification-clinical-use-and-mode-of-action/">Cephalosporin</a></h2>
<h2>3. Monobactams:</h2>
<p><img decoding="async" class="aligncenter  wp-image-1329" src="http://www.onlinebiologynotes.com/wp-content/uploads/2018/04/monobactam-antibiotics.gif" alt="" width="454" height="387" /></p>
<ul>
<li>The most common example of monobactam is Aztreonam. Monobactam are active against β-lactamase producing Gram –ve Enteric bacteria, Pseudomonas and Serratia. They have extended gram –ve coverage than penicillin. However they are inactive gram +ve bacteria and anaerobes.</li>
<li>Individuals who are allergic to penicillin are usually not allergic to monobactams</li>
<li>Monobactams binds to Penicillin binding protein (PBP) and inhibits transpeptidase activity causing filamentation of bacteria which dies later.</li>
</ul>
<p>list of monobactam antibiotics</p>
<ul>
<li>Azteronam</li>
<li>Tigemonam</li>
<li>carumonam</li>
<li>Nocardicin A</li>
</ul>
<h2>4. Carbapenems:</h2>
<p><img decoding="async" class="aligncenter  wp-image-1330" src="http://www.onlinebiologynotes.com/wp-content/uploads/2018/04/carbapenems.jpg" alt="" width="463" height="450" srcset="https://www.onlinebiologynotes.com/wp-content/uploads/2018/04/carbapenems.jpg 1300w, https://www.onlinebiologynotes.com/wp-content/uploads/2018/04/carbapenems-300x291.jpg 300w, https://www.onlinebiologynotes.com/wp-content/uploads/2018/04/carbapenems-768x746.jpg 768w, https://www.onlinebiologynotes.com/wp-content/uploads/2018/04/carbapenems-1024x995.jpg 1024w" sizes="(max-width: 463px) 100vw, 463px" /></p>
<ul>
<li>Carbapenems are broad spectrum drug, virtually active against every bacteria. They are active against Gram +ve and Gram –ve bacteria including <em>Pseudomonas</em>, <em>Serratia</em>, indole positive <em>Proteus</em> and <em>Bacteroid</em> <em>fragellis</em>. Carbapenems are resistant to hydrolysis by β-lactamases.</li>
</ul>
<p>Example ofcarbapenems:</p>
<ul>
<li>Thienamycin</li>
<li>Imipenem</li>
<li>Mezopenem</li>
<li>Ertapenem</li>
<li>Imipenem can be hydrolysed by dihydropeptidase found in renal tubules in Human, so imipenem should be administered along with dihydropeptidase inhibitors (Cilastatin).</li>
<li>Meropenem and ertapenem are resiatant to hydrolyse by dihydroxypeptidase.</li>
<li>Individuals allergic to penicillin should not be recommended Carbapenem drugs.</li>
<li>Bacteria producing metallo-β-lactamase such as Stenotrophomonas metophila and Bacteroids fragillis are resistant to carbapenems.</li>
</ul>
<h2>5. Clavulanic acid:</h2>
<p><img loading="lazy" decoding="async" class="aligncenter  wp-image-1331" src="http://www.onlinebiologynotes.com/wp-content/uploads/2018/04/Clavulanic-Acid.png" alt="" width="220" height="180" srcset="https://www.onlinebiologynotes.com/wp-content/uploads/2018/04/Clavulanic-Acid.png 720w, https://www.onlinebiologynotes.com/wp-content/uploads/2018/04/Clavulanic-Acid-300x246.png 300w" sizes="auto, (max-width: 220px) 100vw, 220px" /></p>
<ul>
<li>Clavulanic acid is a β-lactamase inhibitors. The resistant strain of bacteria producing βlactamase enzyme hydrolyse β-lactam antibiotics and become resistant.</li>
<li>β-lactamase inhibitors have special property of inhibiting activity of β-lactamase. They are also β-lactam group of antibiotics with very litte antimicrobial activity.</li>
<li>The β-lactamase inhibitors are used in combination with β-lactam antibiotics.</li>
</ul>
<h2>Beta-lactam antibiotics: Penicillin, Cephalosporin, Monobactam, Carbapenems and Clavulanic acid</h2>
<p>The post <a href="https://www.onlinebiologynotes.com/beta-lactam-antibiotics-penicillin-cephalosporin-monobactam-carbapenems-and-clavulanic-acid/">Beta-lactam antibiotics: Penicillin, Cephalosporin, Monobactam, Carbapenems and Clavulanic acid</a> appeared first on <a href="https://www.onlinebiologynotes.com">Online Biology Notes</a>.</p>
]]></content:encoded>
					
		
		
			</item>
	</channel>
</rss>
