Evidence map›Paper›PMID 42193213›Full record

ArticleAntioxidants (Basel, Switzerland)2026

Caffeic Acid Release from Inulin Caffeate: A Comparative Study with Spray-Dried Inulin Microparticles Under Gastrointestinal Digestion.

Patricio Romero-Hasler, Alejandra Quintriqueo-Cid, Begoña Giménez, Eduardo Soto-Bustamante, María Carolina Zúñiga-López, Paz Robert

Abstract read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Patricio Romero-HaslerDepartamento de Ciencia de los Alimentos y Tecnología Química, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, Dr. Carlos Lorca Tobar 964, Independencia, Santiago 81380494, Chile.ORCID 0000-0002-9211-2514
Alejandra Quintriqueo-CidDepartamento de Ciencia de los Alimentos y Tecnología Química, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, Dr. Carlos Lorca Tobar 964, Independencia, Santiago 81380494, Chile.ORCID 0000-0002-2225-1906
Begoña GiménezDepartamento de Ciencia y Tecnología de los Alimentos, Facultad Tecnológica, Universidad de Santiago de Chile, Av. Víctor Jara 3769, Estación Central, Santiago 9170124, Chile.ORCID 0000-0002-9553-6291
Eduardo Soto-BustamanteDepartamento de Química Orgánica y Fisicoquímica, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, Dr. Carlos Lorca Tobar 964, Independencia, Santiago 81380494, Chile.ORCID 0000-0002-0735-5715
María Carolina Zúñiga-LópezDepartamento de Química Inorgánica y Analítica, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, Sergio Livingstone, 1007, Independencia, Santiago 8380492, Chile.
Paz RobertDepartamento de Ciencia de los Alimentos y Tecnología Química, Facultad de Ciencias Químicas y Farmacéuticas, Universidad de Chile, Dr. Carlos Lorca Tobar 964, Independencia, Santiago 81380494, Chile.ORCID 0000-0002-3276-2451

Funding

Agencia Nacional de Investigación y Desarrollo Fondecyt Postdoctoral 3210715Agencia Nacional de Investigación y Desarrollo Fondecyt Regular 1221038Agencia Nacional de Investigación y Desarrollo Fondequip EQM 200266
6 · The paper itself

Abstract

This study compared the physicochemical properties of inulin caffeate, where caffeic acid (CA) was covalently bound to inulin (CA-Inu, degree of substitution: 0.07), with CA spray-dried inulin microparticles (Mp(CA/Inu)), as well as release profiles of CA from CA-Inu and Mp(CA/Inu) under in vitro simulated gastrointestinal digestion. Encapsulation by spray drying was optimized using a Central Composite Design, achieving an encapsulation efficiency of 98%. CA was rapidly released from Mp(CA/Inu) during the oral and gastric phases, followed by a slight decrease in the intestinal phase due to interaction with digestive enzymes. In contrast, no release of CA was detected from CA-Inu during the oral and gastric phases. Approximately 30% was released in the intestinal phase, with a further increase in the colonic phase, especially in the presence of inulinase. This strategy, based on the covalent binding of phenolic compounds to biopolymers, can promote targeted delivery in the later stages of gastrointestinal digestion.

Indexed as

caffeic acidchemical functionalizationinulinin vitro simulated digestionmicroencapsulation

Identifiers

PMID42193213
PMCPMC13203464

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.