Evidence map›Paper›PMID 41992462›Full record

ArticleRecent patents on biotechnology2026

Sushmita Semwal, Neeraj Kumar, Bhuwan Chandra Joshi, Piyush Verma

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Article in Recent patents on biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Sushmita SemwalDepartment of Pharmacology, School of Pharmaceutical Sciences, Shri Guru Ram Rai University, Dehradun-248001, Uttarakhand, India.ORCID 0000-0002-4036-2976
Neeraj KumarDepartment of Pharmacology, School of Pharmaceutical Sciences, Shri Guru Ram Rai University, Dehradun-248001, Uttarakhand, India.ORCID 0000-0002-5584-8522
Bhuwan Chandra JoshiDepartment of Pharmaceutical Sciences, Faculty of Technology, Sir J.C. Bose Technical Campus Bhimtal, Kumaun University Nainital-263 136, Uttarakhand, India.ORCID 0000-0003-4106-1793
Piyush VermaRadiological and Nuclear Decontamination Research Group, Department of CBRN Defence, Institute of Nuclear Medicine and Allied Sciences (INMAS), Defence R&D Organisation, Brig. SK. Mazumdar Marg, Timarpur, New Delhi, 110054, India.ORCID 0000-0002-1342-6452

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe plant Cinnamomum tamala (Buch.-Ham.) T. Nees & C.H. Ebern. (Family: Lauraceae) is commonly known as 'tejpaat' in India, has leaves and bark reported to possess anticancer, immunomodulatory, antidiabetic, and diuretic activities. The objective of the present study was to explore the antitumor potential of the chloroform extract of Cinnamomum tamala leaves (CTCE) in BALB/c mice against Ehrlich's Carcinoma (EC).

methodsBased on preliminary in-vitro cytotoxicity studies, CTCE was selected for an in-vivo antitumor study. Anticancer activity of CTCE was evaluated in BALB/c mice against EC at the doses of 50, 100, 250, and 500 mg/kg body weight. CTCE was administered for 15 consecutive days after induction of the tumor. After 24 hours from the last administered dose and 18 hours of fasting, half of the mice were sacrificed, while the other half was kept alive to evaluate any potential for increasing the lifespan. The antitumor effect of CTCE was assessed by evaluating tumor volume, hematological parameters, and the life span of the EC-bearing host.

resultsCTCE showed a significant decrease (p<0.05) in tumor volume and increased the lifespan of EC tumor-bearing mice in a dose-dependent manner compared with the untreated group. The hematological profile, including RBC count, hemoglobin, WBC count, and DLC, was also improved upon treatment. DISCUSSION: C. tamala chloroform extract (CTCE) showed significant anticancer potential by reducing cell viability, inhibiting tumor growth, and prolonging survival without toxicity, suggesting it as a promising source of bioactive compounds for anticancer drug development.

conclusionThe results suggest that CTCE exhibits dose-dependent anticancer activity in comparison with EC control mice and demonstrates significant effects relative to doxorubicin. Its antitumor activity may be attributed to the presence of active constituents within the extract. This investigation also highlights recent advancements in intellectual property rights and patent strategies related to plant-derived anticancer agents.

Indexed as

Antineoplastic Agents, PhytogenicCarcinoma, Ehrlich TumorCinnamomumPlant ExtractsPlant LeavesAnimalsCell Line, TumorFemaleMaleMiceMice, Inbred BALB CAntineoplastic Agents, PhytogenicPlant Extractsantioxidantantitumorbioactive compoundsCinnamomum tamaladoxorubicinEhrlich’s Carcinoma

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.