<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Endang Ariyani Setyowati</style></author><author><style face="normal" font="default" size="100%">Alim Isnansetyo</style></author><author><style face="normal" font="default" size="100%">Tjut Sugandawaty Djohan</style></author><author><style face="normal" font="default" size="100%">Raden Wisnu Nurcahyo</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antimalarial Activity of Microalgae Extracts Based on Inhibition of PfMQO, a Mitochondrial Plasmodium falciparum Enzyme</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antimalarial</style></keyword><keyword><style  face="normal" font="default" size="100%">Inhibitory activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Microalgae</style></keyword><keyword><style  face="normal" font="default" size="100%">P falciparum</style></keyword><keyword><style  face="normal" font="default" size="100%">Screening</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">November 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">1477-1482</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Malaria is an important global disease that threatened human life. The resistance&lt;em&gt; Plasmodium &lt;/em&gt;sp. to the available medicines encourages the search for new antimalarial substances based on new mechanisms on the inhibition of PfMQO (the mitochondrial&lt;em&gt; Plasmodium falciparum&lt;/em&gt; enzyme). &lt;strong&gt;Objective: &lt;/strong&gt;The purposes of this study was to screen antimalarial substances from microalgae based on the inhibition of PfMQO. &lt;strong&gt;Materials and Methods: &lt;/strong&gt;Five microalgae were extracted by maceration using chloroform pa and ethanol pa. These ten crude extracts obtained were tested for the inhibitory activity against the PfMQO enzyme. &lt;strong&gt;Results:&lt;/strong&gt; The highest inhibitory activity against PfMQO enzyme was chloroform extract of &lt;em&gt;S. costatum&lt;/em&gt; with 91.050% of inhibition and 0.043 μg/mL of IC&lt;sub&gt;50&lt;/sub&gt;. The ethanol extract of &lt;em&gt;S. platensis &lt;/em&gt;showed 91.999% and 5.25 μg/mL of inhibition and IC&lt;sub&gt;50&lt;/sub&gt;, respectively. These results indicated that the two extracts provide high antimalarial activity exceeded a theoretical standard of antimalarial bioactive compounds. &lt;strong&gt;Conclusion: &lt;/strong&gt;Chloroform extract of &lt;em&gt;S. costatum&lt;/em&gt; and ethanol extract of &lt;em&gt;S. platensis &lt;/em&gt;are promising sources of antimalarial compounds based on the inhibition of PfMQO.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">6s</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">1477</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Endang Ariyani Setyowati&lt;sup&gt;1,2&lt;/sup&gt;, Alim Isnansetyo&lt;sup&gt;3,&lt;/sup&gt;*, Tjut Sugandawaty Djohan&lt;sup&gt;1&lt;/sup&gt;, Raden Wisnu Nurcahyo&lt;sup&gt;4&lt;/sup&gt;, Erwahyuni Endang Prabandari&lt;sup&gt;5&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Biology, Faculty of Biology, Universitas Gadjah Mada, Jl. Teknika Selatan, Sekip Utara, Yogyakarta 55281, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Biology, Universitas Jenderal Soedirman, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;3&lt;/sup&gt;Department of Fisheries, Faculty of Agriculture, Universitas Gadjah Mada, Jl. Flora, Bulaksumur, Yogyakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;4&lt;/sup&gt;Departement of Parasitology,, Faculty of Veterinary Medicine, Universitas Gadjah Mada, Jl. Fauna 2, Karangmalang, Yogyakarta 55281, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;5&lt;/sup&gt;Biotech Center, Agency for the Assessment and Application of Technology, Jakarta, INDONESIA.&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Muhammad Nursid</style></author><author><style face="normal" font="default" size="100%">Endar Marraskuranto</style></author><author><style face="normal" font="default" size="100%">Azizah Kuswardini</style></author><author><style face="normal" font="default" size="100%">Tjahyo Winanto</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Screening of Tyrosinase Inhibitor, Antioxidant and Cytotoxicity of Dried Sea Cucumber from Tomini Bay, Indonesia</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Cytotoxicity</style></keyword><keyword><style  face="normal" font="default" size="100%">Screening</style></keyword><keyword><style  face="normal" font="default" size="100%">Sea cucumber</style></keyword><keyword><style  face="normal" font="default" size="100%">Tyrosinase inhibitor</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">May 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">555-558</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Background:&lt;/strong&gt; Indonesia, as a tropical country, is one of the important producers of sea cucumbers (beche-de-mer). Sea cucumber is a marine invertebrate that contains attractive bioactive secondary metabolites and these metabolites can be used for health as well as cosmetics. &lt;strong&gt;Objective:&lt;/strong&gt; The aim of the study was to determine the activity of tyrosinase inhibitors, antioxidants, and cytotoxicity of sea cucumber methanolic extract. &lt;strong&gt;Methods:&lt;/strong&gt; Dried sea cucumber samples were taken from Boalemo waters, Tomini Bay, Indonesia. Tyrosinase inhibitor assay was carried out spectrophotometrically using tyrosinase enzymes and L-DOPA as a substrate and antioxidant tests were carried out by DPPH method. Cytotoxicity test against human breast cancer cell line (T47D) was conducted using the MTT assay. &lt;strong&gt;Results:&lt;/strong&gt; The study showed that &lt;em&gt;Bohadschia vitiensis&lt;/em&gt; had the best tyrosinase inhibitor activity with IC&lt;sub&gt;50&lt;/sub&gt; value of 0.28 mg/ml. The DPPH free radical scavenging testing showed that all sea cucumbers had weak antioxidant activity. On the other hand, cytotoxicity assay revealed that several sea cucumbers had good cytotoxicity against T47D cells, where &lt;em&gt;Holothuria atra&lt;/em&gt; and &lt;em&gt;Bohadschia marmorata &lt;/em&gt;showed strong cytotoxicities with IC&lt;sub&gt;50&lt;/sub&gt; values of 23.0 and 28.1 ug/mL, respectively. &lt;strong&gt;Conclusion:&lt;/strong&gt; Based on the study, it can be concluded that the dried sea cucumber from the Tomini bay region, Indonesia, has the potential to be developed as a source of tyrosinase inhibitors and cytotoxic agents.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">555</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Muhammad Nursid&lt;sup&gt;1,*&lt;/sup&gt;, Endar Marraskuranto&lt;sup&gt;1&lt;/sup&gt;, Azizah Kuswardini&lt;sup&gt;2&lt;/sup&gt;, Tjahyo Winanto&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Research Center for Marine and Fisheries Product Processing and Biotechnology, Ministry of Marine and Fisheries Affairs, REPUBLIC OF INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Marine and Fisheries Science, University of Jenderal Soedirman, Purwokerto, INDONESIA&lt;/p&gt;
</style></auth-address></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shaik Aminabee</style></author><author><style face="normal" font="default" size="100%">Atmakuri Lakshmana Rao</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Maram Chinna Eswaraiah</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Hepatoprotective Activity of Michelia nilagirica against Paracetamol Induced Hepatic Injury in Rats</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Albino rats</style></keyword><keyword><style  face="normal" font="default" size="100%">Hepatoprotective</style></keyword><keyword><style  face="normal" font="default" size="100%">Michelia nilagirica</style></keyword><keyword><style  face="normal" font="default" size="100%">Paracetamol</style></keyword><keyword><style  face="normal" font="default" size="100%">Screening</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jul-Aug 2015</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">228-235</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Background:&lt;/strong&gt; Michelia nilagirica belonging to the family Mangoliaceae is commonly used by many traditional healers in most of the herbal preparations for diabetes and kidney diseases. &lt;strong&gt;Objective: &lt;/strong&gt;Different fractions isolated from ethanolic extract of whole plant of Michelia nilagirica is investigated for hepatoprotective activity in wistar albino rats against paracetamol induced hepatic injury. &lt;strong&gt;Materials &amp;amp; Methods:&lt;/strong&gt; Rats were divided into eight groups. Each group contains six animals. Hepatic injury was achieved by injecting paracetamol at a dose of 2 mg/kg p.o. &lt;strong&gt;Results:&lt;/strong&gt; The hepatoprotective action is seen with fraction A by reduction in serum marker enzymes like Aspartate transaminase (AST), Alanine transaminase (ALT). It also reduced the elevated levels of Alkaline phosphotase (ALP) &amp;amp; Serum bilirubin. &lt;strong&gt;Conclusion:&lt;/strong&gt; Histopathological studies further confined the hepatoprotective activity of fraction A against paracetamol treated group. The results obtained were compared with silymarin (100 mg/kg, orally), a standard drug.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">228</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p&gt;&lt;strong&gt;Shaik Aminabee&lt;sup&gt;1&lt;/sup&gt;, Atmakuri Lakshmana Rao&lt;sup&gt;*1&lt;/sup&gt; and Maram Chinna Eswaraiah&lt;sup&gt;2 1&lt;/sup&gt;&lt;/strong&gt;Department of Pharmacology, V. V. Institute of Pharmaceutical Sciences, Gudlavalleru, Andhra Pradesh, INDIA 2Department of Pharmacognosy, Anurag College of Pharmacy, Kodad, Telangana, INDIA.&lt;/p&gt;
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