Evidence map›Paper›PMID 36501507›Full record

ArticlePolymers2022

Microencapsulation of

Daniela Sotomayor-Gerding, José Miguel Troncoso, Katherine Díaz-Riquelme, Karin Mariana Torres-Obreque, Juan Cumilaf, Alejandro J Yañez, Mónica Rubilar

Open access · goldAbstract read
In one paragraph

Article in Polymers, 2022. 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
0.1field-weighted citation impact, top 58% of its field
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, 1 citations in OpenAlex.

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

7 authors at 4 institutions in 2 countries.

Daniela Sotomayor-GerdingPrograma de Doctorado en Ciencias de Recursos Naturales, Universidad de La Frontera, Avenida Francisco Salazar 01145, Box 54-D, Temuco 4811230, Chile.ORCID 0000-0003-1258-6814
José Miguel TroncosoCargill Innovation Center, Camino a Pargua km 57, Colaco km 5, Calbuco 5570130, Chile.
Katherine Díaz-RiquelmeDoctorado en Acuicultura, Programa Cooperativo Universidad de Chile-Universidad Católica del Norte-Universidad Católica de Valparaíso, Macul 7830490, Chile.ORCID 0000-0002-3140-8039
Karin Mariana Torres-ObrequeDepartment of Biochemical and Pharmaceutical Technology, School of Pharmaceutical Sciences, University of São Paulo, São Paulo 05508-000, SP, Brazil.
Juan CumilafDoctorate in Engineering Sciences with Specialization in Bioprocesses, Universidad de La Frontera, Avenida Francisco Salazar 01145, Box 54-D, Temuco 4811230, Chile.ORCID 0000-0002-6053-6574
Alejandro J YañezInterdisciplinary Center for Aquaculture Research (INCAR), Concepción 407007, Chile.ORCID 0000-0002-4619-4600
Mónica RubilarDepartment of Chemical Engineering, Faculty of Engineering and Sciences, Universidad de La Frontera, Avenida Francisco Salazar 01145, Box 54-D, Temuco 4811230, Chile.
Universidad de La Frontera · CLAustral University of Chile · CLPontificia Universidad Católica de Valparaíso · CLUniversidade de São Paulo · BR

Funding

Agencia Nacional de Investigación y Desarrollo Doctoral Scholarship n° 21150735Agencia Nacional de Investigación y Desarrollo FONDEQUIP project EQM 130028CORFO Project 16 IFI-57790, Ewos Fish Health CenterFONDAP INCAR 15110027
6 · The paper itself

Abstract

The development of fish oral vaccines is of great interest to the aquaculture industry due to the possibility of rapid vaccination of a large number of animals at reduced cost. In a previous study, we evaluated the effect of alginate-encapsulated Piscirickettsia salmonis antigens (AEPSA) incorporated in feed, effectively enhancing the immune response in Atlantic salmon (Salmo salar). In this study, we seek to characterize AEPSA produced by ionic gelation using an aerodynamically assisted jetting (AAJ) system, to optimize microencapsulation efficiency (EE%), to assess microparticle stability against environmental (pH, salinity and temperature) and gastrointestinal conditions, and to evaluate microparticle incorporation in fish feed pellets through micro-CT-scanning. The AAJ system was effective in obtaining small microparticles (d < 20 μm) with a high EE% (97.92%). Environmental conditions (pH, salinity and temperature) generated instability in the microparticles, triggering protein release. 62.42% of the protein content was delivered at the intestinal level after in vitro digestion. Finally, micro-CT-scanning images confirmed microparticle incorporation in fish feed pellets. In conclusion, the AAJ system is effective at encapsulating P. salmonis antigens in alginate with a high EE% and a size small enough to be incorporated in fish feed and produce an oral vaccine.

Indexed as

alginateantigenencapsulation efficiencyfish feedMicro-CT-scanningoral vaccineparticle sizePiscirickettsia salmonisstabilityvacuum coating

Identifiers

PMID36501507
PMCPMC9741032
OpenAlexW4310038864

What OpenQuestion 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 OpenQuestion graph.