<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(1)</volume><submitter>Azzazy HME</submitter><pubmed_abstract>This work aims to develop and optimize blended polylactide-&lt;i>co&lt;/i>-glycolide (PLGA) and poly(ε-caprolactone, PCL) loaded with &lt;i>Boswellia sacra&lt;/i> oil (BO) to improve BO's physicochemical properties and anti-breast cancer effects &lt;i>via&lt;/i> enhancing apoptosis. In this context, BO was extracted from &lt;i>B. sacra&lt;/i> oleo gum resins (BO) &lt;i>via&lt;/i> hydrodistillation and chemically characterized by evaluating its essential oil's composition using gas chromatography-mass spectrometry. Then, BO/PLGA-PCL NPs were formulated using the emulsion (O/W) solvent evaporation technique using a PLGA-PCL mixture at five different ratios (1:1, 2:1, 3:1, 1:2, and 1:3, respectively). The optimized NPs had a spherical morphology with no agglomerations and the lowest hydrodynamic size (230.3 ± 3.7 nm) and polydispersity index (0.13 ± 0.03) and the highest ζ potential (-20.36 ± 4.89 mV), as compared to the rest of the formulas. PLGA-PCL NPs could entrap 80.59 ± 3.37% of the BO and exhibited a controlled, sustained release of BO (83.74 ± 3.34%) over 72 h. Encapsulating BO in the form of BO/PLGA-PCL NPs resulted in a lower IC&lt;sub>50&lt;/sub> value as assessed by the MTT assay. Furthermore and upon assessing the apoptotic effect of both BO and BO/PLGA-PCL NPs, there was an increase in the percentage of apoptotic and necrotic cell percentages compared to the control and free BO. Encapsulation of BO in PLGA-PCL NPs doubled the percentage of apoptotic and necrotic cells exerted by free BO. These findings support the potential use of BO/PLGA-PCL NPs in treating breast cancer.</pubmed_abstract><journal>ACS omega</journal><pagination>1017-1025</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9835537</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Essential Oils Extracted from &lt;i>Boswellia sacra&lt;/i> Oleo Gum Resin Loaded into PLGA-PCL Nanoparticles: Enhanced Cytotoxic and Apoptotic Effects against Breast Cancer Cells.</pubmed_title><pmcid>PMC9835537</pmcid><pubmed_authors>Elhusseiny M</pubmed_authors><pubmed_authors>Sawy AM</pubmed_authors><pubmed_authors>Mahdy NK</pubmed_authors><pubmed_authors>Shamma SN</pubmed_authors><pubmed_authors>Azzazy HME</pubmed_authors><pubmed_authors>Al Mulla H</pubmed_authors><pubmed_authors>Abdelnaser A</pubmed_authors><pubmed_authors>Alwahibi S</pubmed_authors><pubmed_authors>Fahmy SA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Essential Oils Extracted from &lt;i>Boswellia sacra&lt;/i> Oleo Gum Resin Loaded into PLGA-PCL Nanoparticles: Enhanced Cytotoxic and Apoptotic Effects against Breast Cancer Cells.</name><description>This work aims to develop and optimize blended polylactide-&lt;i>co&lt;/i>-glycolide (PLGA) and poly(ε-caprolactone, PCL) loaded with &lt;i>Boswellia sacra&lt;/i> oil (BO) to improve BO's physicochemical properties and anti-breast cancer effects &lt;i>via&lt;/i> enhancing apoptosis. In this context, BO was extracted from &lt;i>B. sacra&lt;/i> oleo gum resins (BO) &lt;i>via&lt;/i> hydrodistillation and chemically characterized by evaluating its essential oil's composition using gas chromatography-mass spectrometry. Then, BO/PLGA-PCL NPs were formulated using the emulsion (O/W) solvent evaporation technique using a PLGA-PCL mixture at five different ratios (1:1, 2:1, 3:1, 1:2, and 1:3, respectively). The optimized NPs had a spherical morphology with no agglomerations and the lowest hydrodynamic size (230.3 ± 3.7 nm) and polydispersity index (0.13 ± 0.03) and the highest ζ potential (-20.36 ± 4.89 mV), as compared to the rest of the formulas. PLGA-PCL NPs could entrap 80.59 ± 3.37% of the BO and exhibited a controlled, sustained release of BO (83.74 ± 3.34%) over 72 h. Encapsulating BO in the form of BO/PLGA-PCL NPs resulted in a lower IC&lt;sub>50&lt;/sub> value as assessed by the MTT assay. Furthermore and upon assessing the apoptotic effect of both BO and BO/PLGA-PCL NPs, there was an increase in the percentage of apoptotic and necrotic cell percentages compared to the control and free BO. Encapsulation of BO in PLGA-PCL NPs doubled the percentage of apoptotic and necrotic cells exerted by free BO. These findings support the potential use of BO/PLGA-PCL NPs in treating breast cancer.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-18T13:24:46.523Z</modification><creation>2025-04-06T23:04:00.616Z</creation></dates><accession>S-EPMC9835537</accession><cross_references><pubmed>36643489</pubmed><doi>10.1021/acsomega.2c06390</doi></cross_references></HashMap>