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The Effect of Nanoliposomal Curcumin (Cur-NLPs) Proliferation Rate with Cell Counting Kit 8 (CCK-8) and PI3K expression in cervical cancer HeLa cells
Universa Medicina · Vol. 45 No. 2 (2026) · hlm. 249–258
ISSN 2407-2230, 1907-3062
Terbit 2026-07-21
Penerbit Faculty of Medicine, Universitas Trisakti
Bahasa eng
Abstrak
INTRODUCTIONCervical cancer is a major health problem in developing countries. Cisplatin therapy has limitations related to toxicity and drug resistance associated with activation of the PI3K/AKT/mTOR pathway. Curcumin has anticancer activity, but its bioavailability is low; therefore, it has been developed in a nanoliposomal formulation. This study aimed to evaluate the effects of curcumin nanoliposomes (Cur-NLPs) on proliferation and PI3K expression of HeLa cells. METHODSAn experimental study was conducted using HeLa cells, divided into seven groups: negative control, cisplatin 5 µg/mL, and Cur-NLPs groups at 50, 100, 150, 200, and 250 µg/mL. Cell viability was measured using the cell counting kit-8 (CCK-8). Measurements were performed at 24 and 48 hours at a wavelength of 450 nm. Based on viability results, PI3K expression was analyzed at 48 hours using flow cytometry in five groups: negative control, cisplatin, and Cur-NLPs at 100, 150, and 200 µg/mL. Data were analyzed using one-way ANOVA followed by Games-Howell test. RESULTSCur-NLPs significantly reduced HeLa cell viability at 24 and 48 hours (p<0.001). The 200 µg/mL dose showed the most optimal antiproliferative effect, with viability of 38.3% at 24 hours and 18.0% at 48 hours. PI3K expression in the Cur-NLPs group (42.49–45.03%) was lower than that in the cisplatin group (66.78%), but the difference was not statistically significant (p=0.063). CONCLUSIONCur-NLPs inhibited HeLa cell viability in a dose- and time-dependent manner and showed a trend toward reduced PI3K expression. Further replication and analysis of downstream PI3K markers are needed to confirm these findings.
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University of Brawijaya State University of Malang RSUD Prof. Dr. Saiful Anwar Malang
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Sumber metadata: OAI-PMH (metadata jurnal) https://univmed.org/ejurnal/index.php/medicina/oai, pertama di-harvest 10 Nov 2026, terakhir terlihat 10 Nov 2026.
Metadata asli (oai_dc)
<oai_dc:dc xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
<dc:title xml:lang="en">The Effect of Nanoliposomal Curcumin (Cur-NLPs) Proliferation Rate with Cell Counting Kit 8 (CCK-8) and PI3K expression in cervical cancer HeLa cells</dc:title>
<dc:creator xml:lang="en"> Subandi, Subandi</dc:creator>
<dc:creator xml:lang="en">Suciati, Ferry</dc:creator>
<dc:creator xml:lang="en">Arifiandi, Maya Devi </dc:creator>
<dc:creator xml:lang="en">Indrawan, I Wayan Agung </dc:creator>
<dc:subject xml:lang="en">Nanoliposomal curcumin</dc:subject>
<dc:subject xml:lang="en">HeLa cells</dc:subject>
<dc:subject xml:lang="en">cervical cancer</dc:subject>
<dc:subject xml:lang="en">cell proliferation</dc:subject>
<dc:subject xml:lang="en">PI3K</dc:subject>
<dc:subject xml:lang="en">flow cytometry</dc:subject>
<dc:description xml:lang="en">INTRODUCTIONCervical cancer is a major health problem in developing countries. Cisplatin therapy has limitations related to toxicity and drug resistance associated with activation of the PI3K/AKT/mTOR pathway. Curcumin has anticancer activity, but its bioavailability is low; therefore, it has been developed in a nanoliposomal formulation. This study aimed to evaluate the effects of curcumin nanoliposomes (Cur-NLPs) on proliferation and PI3K expression of HeLa cells.
METHODSAn experimental study was conducted using HeLa cells, divided into seven groups: negative control, cisplatin 5 µg/mL, and Cur-NLPs groups at 50, 100, 150, 200, and 250 µg/mL. Cell viability was measured using the cell counting kit-8 (CCK-8). Measurements were performed at 24 and 48 hours at a wavelength of 450 nm. Based on viability results, PI3K expression was analyzed at 48 hours using flow cytometry in five groups: negative control, cisplatin, and Cur-NLPs at 100, 150, and 200 µg/mL. Data were analyzed using one-way ANOVA followed by Games-Howell test.
RESULTSCur-NLPs significantly reduced HeLa cell viability at 24 and 48 hours (p&lt;0.001). The 200 µg/mL dose showed the most optimal antiproliferative effect, with viability of 38.3% at 24 hours and 18.0% at 48 hours. PI3K expression in the Cur-NLPs group (42.49–45.03%) was lower than that in the cisplatin group (66.78%), but the difference was not statistically significant (p=0.063).
CONCLUSIONCur-NLPs inhibited HeLa cell viability in a dose- and time-dependent manner and showed a trend toward reduced PI3K expression. Further replication and analysis of downstream PI3K markers are needed to confirm these findings.</dc:description>
<dc:publisher xml:lang="en">Faculty of Medicine, Universitas Trisakti</dc:publisher>
<dc:date>2026-07-21</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
<dc:format>application/pdf</dc:format>
<dc:identifier>https://univmed.org/ejurnal/index.php/medicina/article/view/1954</dc:identifier>
<dc:identifier>10.18051/UnivMed.2026.v45.249-258</dc:identifier>
<dc:source xml:lang="en">Universa Medicina; Vol. 45 No. 2 (2026); 249-258</dc:source>
<dc:source>2407-2230</dc:source>
<dc:source>1907-3062</dc:source>
<dc:source>10.18051/UnivMed.2026.v45.i2</dc:source>
<dc:language>eng</dc:language>
<dc:relation>https://univmed.org/ejurnal/index.php/medicina/article/view/1954/882</dc:relation>
<dc:rights xml:lang="en">Copyright (c) 2026 Subandi Subandi, Ferry Suciati, Maya Devi Arifiandi, I Wayan Agung Indrawan</dc:rights>
<dc:rights xml:lang="en">https://creativecommons.org/licenses/by-nc-sa/4.0</dc:rights>
</oai_dc:dc>
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APA 7
Subandi, S., Suciati, F., Arifiandi, M. D., & Indrawan, I. W. A. (2026). The Effect of Nanoliposomal Curcumin (Cur-NLPs) Proliferation Rate with Cell Counting Kit 8 (CCK-8) and PI3K expression in cervical cancer HeLa cells. Universa Medicina, 45(2), 249–258. https://doi.org/10.18051/UnivMed.2026.v45.249-258
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S. Subandi, F. Suciati, M. D. Arifiandi, and I. W. A. Indrawan, “The Effect of Nanoliposomal Curcumin (Cur-NLPs) Proliferation Rate with Cell Counting Kit 8 (CCK-8) and PI3K expression in cervical cancer HeLa cells,” Universa Medicina, vol. 45, no. 2, pp. 249–258, 2026, doi: 10.18051/UnivMed.2026.v45.249-258.
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