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<article>
<front>
<journal-meta>
<journal-id journal-id-type='publisher'>IJRAP</journal-id>
<journal-title>International Journal of Research in Ayurveda and Pharmacy</journal-title>
<issn pub-type='ppub'>2277-4343</issn>
 <publisher>
<publisher-name>Moksha Publishing House </publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type='other'>10.7897/2277-4343.17251</article-id>
<title-group>
<article-title>APOPTOSIS-DRIVEN ANTI-LEUKEMIC EFFECTS OF A POLYHERBAL COMBINATION: BIOLOGICAL ACTIVITY AND CHEMICAL CHARACTERIZATION
</article-title>
</title-group>
<contrib-group>
<contrib contrib-type='author'>
<name>Prerona Boruah *</name>
</contrib>
<contrib contrib-type='author'>
<name> Sanjay Ghosh Dastidar</name>
</contrib>
<contrib contrib-type='author'>
<name> Shanmukh Malineni</name>
</contrib>
</contrib-group>
<pub-date>
<month>11</month>
<year>-0001</year>
</pub-date>
<fpage>59</fpage>
<lpage>63</lpage>
<abstract><title>Abstract</title>
Hematologic malignancies impose a major burden in India; while modern therapies improve survival, toxicity, relapse, and cost limit benefit. We investigated a proprietary Ayurvedic preparation used clinically as a 1:1 mixture of an anti-cancer extract (Can-n-Cer-BC) and a supportive formulation (Detoxigab). Chemical profiling by untargeted LCâMS and in-vitro testing (DPPH scavenging, CellTiter-GloÂ® viability, and caspase activity) were performed. LCâMS revealed ~35 features across 3.8â17.0 min with a right-tailed distribution. Several high-area library matches resembled siloxanes/organometallics typical of background; these were treated as provisional and reserved for quality control, whereas lower-abundance features were prioritized as putative phytochemicals. Functionally, the combined extract displayed minimal DPPH activity at ?1,000 __ampersandsignmu;g/mL, rising to ~40% at 2,500 __ampersandsignmu;g/mL and ~55â60% at 10,000 __ampersandsignmu;g/mL. In contrast, at 2,500 __ampersandsignmu;g/mL the extract caused a ~90% loss of ATP-based viability (signal ~10% of control) and increased caspase activity to ~135â140% of control. These findings indicate that antioxidant effects emerge only at high concentrations and are unlikely to account for the steep fall in viability; rather, apoptosis appears to be a principal mechanism of action for the mixture, plausibly mediated by multiple low-abundance phytochemicals acting in concert. Quality-control steps (system blanks, targeted MS/MS with internal standards, replicate extractions, and ICP-MS for metals) were implemented to secure chemical attributions. Overall, the Can-n-Cer-BC/Detoxigab combination exhibits potent, caspase-associated anti-leukemic activity in vitro and warrants dose response, selectivity, mechanistic confirmation (e.g., Annexin V/PI ) and bioassay-guided fractionation to define active principles and enable standardized, safe development as a potential adjunct to blood-cancer care.
</abstract>
<kwd-group>
<title>Keywords</title>
<kwd>Blood cancer</kwd>
<kwd> Ayurveda</kwd>
<kwd> polyherbal extract</kwd>
<kwd> DPPH</kwd>
<kwd> apoptosis</kwd>
<kwd> LC-MS</kwd>
<kwd> RPMI 8226</kwd>
<kwd> caspase 3/7</kwd>
</kwd-group>
<counts><ref-count count='0'/><page-count count='4'/></counts>
</article-meta></front><back><ref-list><title>References</title></ref-list></back></article>
