Szczegóły publikacji

Opis bibliograficzny

Design of the manufacturing conditions to increase curcumin loading in polyanhydride microparticles / Julie Borreau, Konrad KWIECIEŃ, Anna KUSIBAB, Elżbieta PAMUŁA // Engineering of Biomaterials [Dokument elektreoniczny]. — Czasopismo elektroniczne ; ISSN  3071-7825 . — Tytuł poprz.: Inżynieria Biomateriałów = Engineering of Biomaterials ; ISSN:  1429-7248. — 2025 — vol. 173 art. no. 14, s. 1–7. — Wymagania systemowe: Adobe Reader. — Bibliogr. s. 7, Abstr. — Publikacja dostępna online od: 2025-12-03

Autorzy (4)

Słowa kluczowe

curcumindrug delivery systempoly(sebacic anhydride)polymeric microparticlestrichloroacetic acid

Dane bibliometryczne

ID BaDAP170206
Data dodania do BaDAP2026-09-23
Tekst źródłowyURL
DOI10.34821/eng.biomat.173.2025.14
Rok publikacji2025
Typ publikacjiartykuł w czasopiśmie
Otwarty dostęptak
Creative Commons
Czasopismo/seriaInżynieria Biomateriałów = Engineering of Biomaterials

Abstract

Curcumin is a natural polyphenol with anti-inflammatory and anticancer potential, but its poor aqueous solubility and limited incorporation into polymeric carriers hinder clinical translation. Covalent or ion-paired conjugation with a polymeric matrix may enhance drug retention and loading, thereby improving delivery efficiency. This study investigated whether introducing acidic conditions to oil-in-water emulsification would promote curcumin–polyanhydride conjugation and improve encapsulation efficiency (EE) and drug loading (DL) in poly(sebacic anhydride) (PSA) microparticles (MPs). The results obtained by fluorimetry show that encapsulation outcomes strongly depended on the acid used. Trifluoroacetic acid (TFA) yielded negligible curcumin incorporation, with EE ranging from 1.7 ± 0.1% to 19.7 ± 0.6% and DL between 0.28 ± 0.01% and 3.3 ± 0.1%. In contrast, hydrochloric acid (HCl) and sulfuric acid (H2SO4) produced results comparable to non-acidified controls, with EE around 30–35% and DL around 5–6%. A markedly different outcome was observed with 2% aqueous trichloroacetic acid (TCA). Condition X21 exhibited the best performance with 53.6 ± 0.5% (EE) and 8.9 ± 0.1% (DL), while another TCA-based formulation (X20) also showed high encapsulation values (EE = 45.5 ± 1.1%, DL = 7.6 ± 0.2%). However, despite this significant improvement in curcumin incorporation, TCA-derived MPs compromised L929 fibroblasts viability, whereas HCl- and H2SO4- treated formulations were cytocompatible. These findings demonstrate that low-concentration aqueous TCA enhances curcumin incorporation into PSA MPs, likely via conjugate formation, but compromises cytocompatibility due to residual TCA. Further optimization of TCA concentration and purification steps will be necessary to balance drug loading with safety for biomedical applications.

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