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<title>European Journal of Pharmaceutical Sciences 1 March 2025</title>
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<dateIssued>2025</dateIssued>
<issuance>monographic</issuance>
<edition>1 March 2025</edition>
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<languageTerm type="text">Indonesia</languageTerm>
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<note>ABSTRACT
Triple-negative breast cancer (TNBC) presents with resistance phenotypes to certain therapies, such as cisplatin,
often requiring higher dosing, with associated acquired tumor resistance, renal toxicity, and variable patient

responses. A self-emulsifying drug delivery (SEDD) formulation approach was proposed to overcome the limi-
tations of cisplatin in TNBC, focusing on improving intracellular cisplatin and control siRNA uptake as a proof-of-
principle of dual drug delivery. Four SEDD formulations were prepared and optimized for cisplatin (o/w)

emulsion and FITC-siRNA (w/o) emulsion using pseudo-ternary phase diagrams to facilitate the formation of

water-in-oil-water (w/o/w) emulsions. Formulations were characterized by size, polydispersity (PDI), and sur-
face charge and tested in vitro. Cellular uptake via triplex staining of drug-loaded SEDDs was investigated. SEDDs

showed enhanced internalization and promoted selective TNBC cellular uptake. The current study is a proof-of- principle for the successful co-delivery of cisplatin (small molecule) and siRNA (large molecule) via the SEDDs platform.</note>
<subject authority=""><topic>apoptosis</topic></subject>
<subject authority=""><topic>Triple-negative breast cancer (TNBC)</topic></subject>
<subject authority=""><topic>drug delivery</topic></subject>
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<sublocation>Perpus.Akfarsam (Jurnal Farmasi Internasional)</sublocation>
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