Evidence map›Paper›PMID 40225228›Full record

ArticleAdvances in pharmacological and pharmaceutical sciences2025

Spray-Dried Powders of Casein-Encapsulated Rutin Stabilized With Sugars for the Enhancement of Intestinal Drug Solubility.

Helmy Yusuf, Sinta Choirunissa Fitriana, Ni Luh Eradeasty Putri Darmawan, Revalida Ainun Nisa, Retno Sari, Dwi Setyawan

Abstract read
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Article in Advances in pharmacological and pharmaceutical sciences, 2025. 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

6 authors.

Helmy YusufDepartment of Pharmaceutical Sciences, Faculty of Pharmacy, Airlangga University, Surabaya 60115, Indonesia.ORCID https://orcid.org/0000-0001-5929-4726
Sinta Choirunissa FitrianaDepartment of Pharmaceutical Sciences, Faculty of Pharmacy, Airlangga University, Surabaya 60115, Indonesia.
Ni Luh Eradeasty Putri DarmawanDepartment of Pharmaceutical Sciences, Faculty of Pharmacy, Airlangga University, Surabaya 60115, Indonesia.
Revalida Ainun NisaDepartment of Pharmaceutical Sciences, Faculty of Pharmacy, Airlangga University, Surabaya 60115, Indonesia.
Retno SariDepartment of Pharmaceutical Sciences, Faculty of Pharmacy, Airlangga University, Surabaya 60115, Indonesia.ORCID https://orcid.org/0000-0002-3391-1877
Dwi SetyawanDepartment of Pharmaceutical Sciences, Faculty of Pharmacy, Airlangga University, Surabaya 60115, Indonesia.ORCID https://orcid.org/0000-0001-8009-6054

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Numerous therapeutic potentials of rutin (RUT) including cardioprotective, neuroprotective, and antihypertension activities have attracted many studies to bring it into clinical use. RUT is phytochemically derived from plants such as apples and tea. It is poorly soluble and very sensible to acidic pH in the stomach environment which leads to conceded oral bioavailability. In contrast, RUT is better soluble in basic environment, thus, encapsulating RUT within enteric microparticles (RUT-MP) using casein (CAS) resolved such problems. The encapsulation by spray-drying employed sugars (lactose, sucrose, and maltodextrin) as bulking agents and for stabilization of the amorphous drug. The developed RUT-MP formulations were prepared in two groups i.e., lower and higher RUT concentrations. The solid states were studied by X-ray diffraction (XRD), differential thermal analysis (DTA) and scanning electron microscopy (SEM). Solubility tests were also carried out on the samples to examine the outcome of the engineered physical modification. The results showed that the RUT-MPs were spherical in morphology. The RUT was transformed into amorphous structure as suggested by the XRD and DTA results indicating that RUT was molecularly dispersed in the RUT-MP. There were no phase separations that occurred as confirmed by the DTA data. Solubility tests carried out on the RUT-MPs showed that the encapsulation with CAS in group with higher concentration of RUT prevented the drug against recovery of the crystallinity and phase separations. The solubility test revealed various substantial enhancements of RUT solubility of the RUT-MPs at pH 7.0. The highest enhancement of RUT solubility was 191,5-fold, with respect to pure RUT. The presence of sugars was beneficial as they improved the yield percentage and might have contributed to the prevention of nano-crystal aggregation which made them a determining aspect for the successful application of spray-dried encapsulation.

Identifiers

PMID40225228
PMCPMC11991810

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