631 research outputs found
Miristato de miristilo “100% natural”. Estudio del proceso de síntesis biocatalítica
El miristato de miristilo es uno de los ésteres cerosos másutilizados en las formulaciones cosméticas como emoliente.La legislación europea permite catalogar como productosnaturales a todos aquellos obtenidos directamente dela naturaleza o los sintetizados mediante procedimientosbiocatalíticos. En este contexto, el presente trabajo recogelos estudios realizados para optimizar la síntesis biocatalíticade miristato de miristilo con lipasa de Candida antarcticainmovilizada (Novozym® 435). Operando a 70ºC, avacío y con circulación de N2 seco, se ha podido obtener,en tan sólo 2 horas, un éster que presenta las mismas características (número ácido, valor de hidroxilo, índice deyodo e índice de saponificación), que los productos quese encuentran actualmente en el mercado, con la notableventaja de que este miristato de miristilo permite el etiquetadode los productos cosméticos que lo contienen como“100% natural”
Sphincter damage during fistulotomy for perianal fistulae and its relationship with faecal incontinence
Background The length of sphincter which can be divided during fistulotomy for perianal fistula is unclear. The aim was to quantify sphincter damage during fistulotomy and determine the relationship between such damage with symptoms and severity of faecal incontinence and long-term quality of life (QOL). Methods A prospective cohort study was performed over a 2-year period. Patients with intersphincteric and mid to low transsphincteric perianal fistulas without risk factors for faecal incontinence were scheduled for fistulotomy. All patients underwent 3D endoanal ultrasound (3D-EAUS) pre-operatively and 8 weeks postoperatively. Measurements were taken of pre- and postoperative anal sphincter involvement and division. Anal continence was assessed using the Jorge-Wexner scale and QOL scores pre, 6 and 12 months postoperatively. Results Forty-nine patients were selected. A strong correlation between pre- and postoperative measurements was found p < 0.001. A median length of 41% of the external anal sphincter and 32% of the internal anal sphincter was divided during fistulotomy. Significant differences in mild symptoms of anal continence were found with increasing length of external anal sphincter division. But there was no significant deterioration in continence, soiling, or quality of life scores at the 1-year follow-up. Division of over two-thirds of the external anal sphincter was associated with the highest incontinence rates. Conclusions 3D-EAUS is a valuable tool for quantifying the extent of sphincter involvement pre- and postoperatively. Post-fistulotomy faecal incontinence is mild and increases with increasing length of sphincter division but does not affect long-term quality of life
Development and economic evaluation of an eco-friendly biocatalytic synthesis of emollient esters.
©. This manuscript version is made available under the CC-BY-NC-ND license http://creativecommons.org/licenses/ccby-nc-nd/4.0/
This document is the Accepted version of a Published Work that appeared in final form in [Bioprocess and Biosystems Engineering]. To access the final edited and published work see [https://doi.org/ 10.1007/s00449-019-02243-1]During the last decades the understanding and prospects of enzyme-catalysed reactions
have been massively widened and there are a number of implemented large-scale enzymatic
processes mainly based in the use of commercial biocatalysts. As it might happen that the
same process can be successfully carried out by different commercial lipases, the election
of the biocatalyst must rely on productivity and economic considerations. This work
presents productiveness and direct operation cost evaluation as a key tool for the selection
between two commercial lipase catalysts, the versatile but expensive Novozym® 435 and a
much more economical option, Lipozyme® TL IM, in the synthesis of spermaceti, a mixture
of emollient esters with cosmetic applications. Proving that Novozym® 435 leads to
minimum savings of 10% with respect to the cheapest immobilized derivative, biocatalyst
cost does not appear to be the major contribution to the economics of the processes under
study, due to their great capacity to be recovered and reused. At laboratory scale, the
biggest economic investment is caused by substrates, which can be massively reduced at
industrial scale by using bulk reagents. In such case, energy cost may be the major
contribution to the process economy. This work proposes an optimized process ready to be
scaled-up in order to accurately determine the energetic requirements of the possible
industrial enzymatic synthesis
Green Production of a High-Value Branched-Chain Diester: Optimization Based on Operating Conditions and Economic and Sustainability Criteria
©. This manuscript version is made available under the CC-BY license http://creativecommons.org/licenses/by/4.0/
This document is the Published version of a Published Work that appeared in final form in [Applied Sciences]. To access the final edited and published work see [https://doi.org/ 10.3390/app13106177]Featured Application: In the last years, consumers’ and administrations’ demand for more sustainable products and processes has been increasing. This work develops a new sustainable way to obtain a branched ester for cosmetic applications (neopentylglycol dilaurate) and demonstrates that this new production route can be economically competitive. Branched-chain esters (BCEs) have found a large number of applications in cosmetics. Among them, neopentyl glycol dilaurate (NPGDL) stands out as an emollient, emulsifier, and skin-conditioning agent. This work presents the synthesis of NPGDL in a solvent-free medium using the two most common immobilized lipases: Novozym® 40086 (Rml) and Novozym® 435 (CalB). Results proved that the former biocatalyst has lower activity and certain temperature deactivation, although conversions ≥ 90% were obtained at 60 °C and 7.5% of catalyst. On the other hand, optimal reaction conditions for Novozym® 435 are 3.75% w/w of the immobilized derivative at 80 °C. Under optimal conditions, the process productivities were 0.105 and 0.169 kg NPGDL/L h, respectively. In order to select the best conditions for NPGDL production, studies on the reuse of the derivative and cost estimation have been performed. Economic study shows that biocatalytic processes can be competitive when lipases are reused for five cycles, yielding biocatalyst productivities of 56 and 122 kg NPGDL/kg biocatalyst using Novozym® 40086 and Novozym® 435, respectively. The final choice will be based on both economic and sustainability criteria. Green metric values using both biocatalysts are similar but the product obtained using Novozym® 40086 is 20% cheaper, making this alternative the best option
Abordaje de pacientes con diabetes y obesidad en atención primaria
Aims:
The
aim
of
this
study
is
to
analyse
the
effect
of
pharmacological
and
non-pharmacological
treatment
on
weight
control
in
patients
with
diabetes
and
obesity.
Design:
Epidemiological,
descriptive,
cross-sectional
study.
Site:
Primary
care.
In
11
health
centres
in
Málaga
and
Cádiz
during
April
and
October
2022.
Participants:
281
patients
over
18
years
old
with
type
2
diabetes
and
obesity
are
included.
Main
measurements:
Socio-demographics,
clinical,
treatment
and
lifestyle
habits
variables
were
obtained
from
medical
records
and
personal
interview.
Descriptive
statistics
were
obtained
for
continuous
variables.
Statistical
tests
were
performed
based
on
the
nature
of
the
variables.
Results:
Variables
like
marital
status,
level
of
education
and
occupation,
and
smoking
habit,
shows
differences
regarding
the
sex
(
p
<
0.05).
82.3%
of
those
who
received
education
lost
weight,
compared
to
67.5%
of
lost
weight
who
received
no
health
education
(
p
=
0.004).
GLP1
and
SGLT2
were
more
commonly
prescribed
for
women
(
p
=
0.048),
and
SGLT2
more
commonly
prescribed
for
men
(
p
=
0.047).
Patients
taking
GLP1,
SGLT2
or
both,
regardless
of
sex,
weight
loss
during
the
study
period
was
−
3.1
kg
(SE:
0.60),
while
the
loss
of
those
who
took
other
medications
was
−
1.33
kg
(SE:
0.62).
The
mean
difference
was
1.75
kg
(
p
=
0.046).
Conclusions:
In
terms
of
weight
loss,
obese
diabetics
who
took
GLP1,
SGLT2
or
both
were
2.5
times
more
likely
to
lose
weight
than
those
who
did
not.
Healthy
lifestyle
choices
are
key
to
weight
loss
in
obese
diabetic
patientsPartial funding for open Access charge: Universidad de Málaga / CBU
The MRC1/CD68 ratio is positively associated with adipose tissue lipogenesis and with muscle mitochondrial gene expression in humans
This is an open-access article distributed under the terms of the Creative Commons Attribution License.[Background]: Alternative macrophages (M2) express the cluster differentiation (CD) 206 (MCR1) at high levels. Decreased M2 in adipose tissue is known to be associated with obesity and inflammation-related metabolic disturbances. Here we aimed to investigate MCR1 relative to CD68 (total macrophages) gene expression in association with adipogenic and mitochondrial genes, which were measured in human visceral [VWAT, n = 147] and subcutaneous adipose tissue [SWAT, n = 76] and in rectus abdominis muscle (n = 23). The effects of surgery-induced weight loss were also longitudinally evaluated (n = ).[Results]: MCR1 and CD68 gene expression levels were similar in VWAT and SWAT. A higher proportion of CD206 relative to total CD68 was present in subjects with less body fat and lower fasting glucose concentrations. The ratio MCR1/CD68was positively associated with IRS1gene expression and with the expression of lipogenic genes such as ACACA, FASN and THRSP, even after adjusting for BMI. The ratio MCR1/CD68 in SWAT increased significantly after the surgery-induced weight loss (+44.7%; p = 0.005) in parallel to the expression of adipogenic genes. In addition, SWAT MCR1/CD68ratio was significantly associated with muscle mitochondrial gene expression (PPARGC1A, TFAM and MT-CO3). AT CD206 was confirmed by immunohistochemistry to be specific of macrophages, especially abundant in crown-like structures. [Conclusion]: A decreased ratio MCR1/CD68 is linked to adipose tissue and muscle mitochondrial dysfunction at least at the level of expression of adipogenic and mitochondrial genes. © 2013 moreno-navarrete et al.This work was supported by grant SAF-2009-10461 and grant PI11-00214 from the Ministerio de Economía y Competitividad, Spain.Peer Reviewe
Study of antitumor activity in breast cell lines using silver nanoparticles produced by yeast
In the present article, we describe a study of antitumor activity in breast cell lines using silver nanoparticles (Ag NPs) synthesized by a microbiological method. These Ag NPs were tested for their antitumor activity against MCF7 and T47D cancer cells and MCF10-A normal breast cell line. We analyzed cell viability, apoptosis induction and endocytosis activity of those cell lines and we observed that the effects of the biosynthesized Ag NPs were directly related with the endocytosis activity. Moreover, Ag NPs had higher inhibition efficacy in tumor lines than in normal lines of breast, which is due to the higher endocytic activity of tumor cells comparing to normal cells. In this way, we are demonstrating that biosynthesized Ag NPs can be an alternative for the treatment of tumors.Fil: Ortega, Francisco Gabriel. Universidad de Granada. Centro de Genómica e Investigación Oncológica; EspañaFil: Fernández Baldo, Martín Alejandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico San Luis. Instituto de Química de San Luis; ArgentinaFil: Fernández, Jorge Gastón. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico San Luis. Instituto de Química de San Luis; ArgentinaFil: Serrano, Maria J.. Universidad de Granada. Centro de Genómica e Investigación Oncológica; EspañaFil: Sanz Ferramola, Maria Isabel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico San Luis. Instituto de Química de San Luis; ArgentinaFil: Diaz Mochón, Juan J.. Universidad de Granada. Centro de Genómica e Investigación Oncológica; EspañaFil: Lorente, José Antonio. Universidad de Granada. Centro de Genómica e Investigación Oncológica; EspañaFil: Raba, Julio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico San Luis. Instituto de Química de San Luis; Argentin
Programming of neural progenitors of the adult subependymal zone towards a glutamatergic neuron lineage by neurogenin 2
Although adult subependymal zone (SEZ) neural stem cells mostly generate GABAergic interneurons, a small progenitor population expresses the proneural gene Neurog2 and produces glutamatergic neurons. Here, we determined whether Neurog2 could respecify SEZ neural stem cells and their progeny toward a glutamatergic fate. Retrovirus-mediated expression of Neurog2 induced the glutamatergic lineage markers TBR2 and TBR1 in cultured SEZ progenitors, which differentiated into functional glutamatergic neurons. Likewise, Neurog2-transduced SEZ progenitors acquired glutamatergic neuron hallmarks in vivo. Intriguingly, they failed to migrate toward the olfactory bulb and instead differentiated within the SEZ or the adjacent striatum, where they received connections from local neurons, as indicated by rabies virus-mediated monosynaptic tracing. In contrast, lentivirus-mediated expression of Neurog2 failed to reprogram early SEZ neurons, which maintained GABAergic identity and migrated to the olfactory bulb. Our data show that NEUROG2 can program SEZ progenitors toward a glutamatergic identity but fails to reprogram their neuronal progeny.We are grateful to Ana Beltrán-Arranz and Laia Torres-Masjoan for help with monosynaptic tracing experiments. We are grateful to Dr. Magdalena Götz for support throughout the project. We acknowledge the Microscopy Core Facility of the Institute of Molecular Biology (IMB) in Mainz. This work was supported by a grant from the Wellcome Trust (206410/Z/17/Z). For the purpose of open access, the authors have applied a CC BY public copyright license to any author-accepted manuscript version arising from this submission. Furthermore, this work was supported by grants from the Deutsche Forschungsgemeinschaft to B.B. (CRC1080, project number 221828878; BE 4182 11-1, project number 357058359) and to M.S.B. (LE 4610 1, project number 450131873); the Research Initiative of the State of Rhineland-Palatinate at the Johannes Gutenberg University Mainz (ReALity) to B.B.; the Spanish Ministry of Science and Innovation (MICINN) to S.G. (grants RTI2018-099345-B-I00 and PID2021-128796OB-I00) and F.O. (PID2019-109155RB-I00 and BFU2015- 70067REDC); and the Inneruniversitäre Forschungsförderung Stufe 1 of the Universitätsmedizin Mainz to S.P. N.M. was supported by a fellowship from the Human Frontiers Science Program (LT000646/2015), W.F. by a fellowship from the China Scholarship Council, J.S.-L. by a fellowship from the UCM-Santander (CT82/20-CT83/20), and S.G. by the Ramón y Cajal Programme (RYC-2015-19185)
Neuroplastic and cognitive impairment in substance use disorders: a therapeutic potential of cognitive stimulation
Author manuscriptDrug addiction is a chronic and relapsing disorder in which repeated drug exposure compromises brain neuroplasticity. Brain areas normally involved in learning and goal- directed behaviors become corrupted, which may lead to cognitive deficits that coexist with other addiction symptoms and predict a worse treatment outcome. New learning experiences that are not motivated by drugs may improve both cognitive deficits and drug-induced symptoms by promoting adaptive neuroplastic changes that could alleviate or reverse those involved in addiction. The present review will focus on whether potentiating healthy cognitive function, either by formal cognitive training or non-drug related environmental experiences, could exert beneficial effects in the therapeutics of addiction. Although additional studies are needed, the available clinical and preclinical evidence suggests that cognitive stimulation may provide a valuable adjuvant intervention in drug addiction.This study was funded by grants from the Spanish Ministry of Economy and Competitiveness (Agencia Estatal de Investigación) co-founded by the European Research Development Fund-AEI/FEDER, UE- (PSI2015-73156-JIN to E.C.O.; PSI2017-82604R to L.J.S.), Red de
Trastornos Adictivos (RD16/0017/0001 to F.R.F.), Plan Nacional sobre Drogas, Ministerio de Sanidad, Servicios Sociales e Igualdad (PNSD2015/047 to J.S.) and the University of Málaga (Plan Propio 2017 – ‘Ayudas para proyectos dirigidos por jóvenes investigadores’, PPIT.UMA.B1.2017/38 to P.S.P).
Author P.S.P. holds a ‘Juan de la Cierva-formación’ grant from the Spanish Ministry of Economy, Industry and Competitiveness (code: FJCI-2015-23925). Author D.L.G.M. holds a ‘FPU’ grant from the Spanish Ministry of Education, Culture and Sports (code: FPU13/04819). Authors J.S., A.S. and F.J.P. hold ‘Miguel Servet’ grants (codes: CPII17/00024, CP14/00173 and CP14/00212, respectively) from the National System of Health-Instituto de Salud Carlos- III co-funded by FEDER, UE. Author E.C.O. holds a ‘Jóvenes Investigadores’ grant (code: PSI2015-73156-JIN) from the Spanish Ministry of Economy and Competitiveness (Agencia Estatal de Investigación) co-funded by FEDER, UE
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