263 research outputs found
Standard Resort Hospitality Elements: A Performance and Impact Analysis
No full textWhen customers decide which resort to visit for vacation or leisure needs, their choice is primarily purpose or activity driven. This fact has dictated a research program focusing primarily on understanding these principal attributes. How- ever, recent research has shown that secondary elements standard across resort typologies can also serve an important role in a guests’ experience. In order to build upon our understanding of these complementary resort features, this study utilizes a modified importance performance analysis methodology. By taking into consideration attribute sali- ence, loyalty determinance internal and relative performance, traditional importance-performance results are seg- mented and accompanied by specific recommendations. Results provide a breakdown of 18 standard resort hospitality elements (SRHE) into 16 categories of the modified IPA and how resort managers can redirect attention to attributes that are performing below expected levels or reposition better than expected performing attributes. Discussion focuses on further understanding the results of the study with potential applications in future research
sj-docx-1-tej-10.1177_20417314221109337 – Supplemental material for Engineering Functional Vascularized Beige Adipose Tissue from Microvascular Fragments of Models of Healthy and Type II Diabetes Conditions
No full textSupplemental material, sj-docx-1-tej-10.1177_20417314221109337 for Engineering Functional Vascularized Beige Adipose Tissue from Microvascular Fragments of Models of Healthy and Type II Diabetes Conditions by Francisca M. Acosta, Katerina Stojkova, Jingruo Zhang, Eric Ivan Garcia Huitron, Jean X. Jiang, Christopher R. Rathbone and Eric M. Brey in Journal of Tissue Engineering</p
Early egg traits in Cancer setosus (Decapoda, Brachyura): effects of temperature and female size
No full textPrevious study on Cancer setosus (Molina, 1782) had shown that latitudinal changes in temperature control the number of annual egg masses. This study focused on the effects of pre-oviposition temperature and female size on egg-traits in C. setosus from Northern (Antofagasta 23ºS) and Central-Southern (Puerto Montt 41ºS) Chile. Blastula eggs produced in nature ranged in dry mass (DM) from 9.1 to 15.1 µg, in carbon (C) from 4.8 to 8.4 µg, in nitrogen (N) from 1.0 to 1.6 µg, in C:N ratio between 4.7 and 5.4, and in volume (V) between 152 and 276 mm3 x 10-4 per female. Blastula eggs from females caught early in the reproductive season in Puerto Montt (09/2006) were significantly higher in DM, C, N, and V than those of females caught two months later (11/2006), reflecting a seasonal increase in water temperature. In Puerto Montt “early” and “late” season blastula eggs were about 32% and 20% higher in DM, C, N, and V as eggs from Antofagasta, respectively. Subsequent egg masses produced in captivity in Puerto Montt followed this pattern of smaller eggs with lower DM, C, and N content at higher pre-oviposition temperatures. In Antofagasta no significant difference in DM, C, N and V between eggs produced in nature and subsequent eggs produced in captivity was found and all egg traits were significantly positively affected by maternal size. Reproductive plasticity in C. setosus helps explaining the species wide latitudinal distribution range
Divergent effects of myogenic differentiation and diabetes on the capacity for muscle precursor cell adipogenic differentiation in a fibrin matrix
No full textThe development of ectopic adipose tissue in skeletal muscle is associated with several skeletal muscle and metabolic pathologies, including Type II Diabetes Mellitus. The adipogenic differentiation of muscle precursor cells (MPCs) has been postulated to occur in skeletal muscle in vivo in a three-dimensional (3-D) configuration; therefore, it is appropriate to investigate this phenomenon using 3-D matrices in vitro. The capacity for MPC adipogenic differentiation in a 3-D environment was investigated in fibrin hydrogels by treating MPCs derived from healthy or diabetic animals with adipogenic induction medias that differed in their ability to increase lipid accumulation and activate the expression of genes associated with adipogenic differentiation (peroxisome proliferator-activated receptor gamma (PPARG), adiponectin (ADIPOQ), and fatty acid synthase (FAS)). The capacity for adipogenic differentiation was diminished, but not prevented, if myogenic differentiation preceded MPC exposure to adipogenic induction conditions. Conversely, adipogenic differentiation was greater in hydrogels containing MPCs from diabetic rats as compared to those derived from lean rats, as evidenced by an increase in lipid accumulation and adipogenic gene expression. Collectively, the data herein support a role for the MPCs in adipogenesis in a 3-D environment and that they may contribute to the ectopic accumulation of adipose tissue. The observation that the potential for adipogenic differentiation is maintained even after a period of myogenic differentiation alludes to the possibility that adipogenesis may occur during different phases of muscle development. Finally, the increase in adipogenic differentiation in hydrogels containing MPCs derived from diabetic animals provides strong evidence that a pathological environment in vivo increases their capacity for adipogenesis. (C) 2020 Elsevier Inc. All rights reserved
BIOMATERIAL SYSTEMS WITH PERSISTENT GROWTH FACTOR GRADIENTS IN VIVO FOR TISSUE ENGINEERING APPLICATIONS
No full textTissue engineering aims to develop strategies for the replacement of damaged, injured or missing tissues with biologically compatible substitutes such as bioengineered tissues. However, generating tissues of su cient volume for clinical application requires the formation of stable and extensive vasculature within the tissue constructs. The overall goal of this work is to enhance vascularization using a gradient biomaterial system and apply this research to engineering vascularized bone of clinical size. First, a method was developed to create persistent growth factor gradients with an adjustable gradient magnitude in vivo. This method generated persistent gradients of platelet-derived growth factor (PDGF-BB) within brin/poly (ethylene glycol) (PEG) sca olds. The presence of a growth factor gradient within the system was veri ed in vivo using near-infrared imaging. Also, a computational model was developed to investigate gradient characteristics within the system. Gradient properties can be controlled by varying the degradation rate of the gradient layer components or dose of PDGF-BB delivered. The angiogenic potential of gradient sca olds was tested in rodents using a subcutaneous implantation model. The depth of tissue invasion and density of blood vessels formed in response to the biomaterial increased with dose of the growth factor. The gradient biomaterial system allows formation of persistent gradients that can be in uenced by biomaterial characteristics, and enhances vascularization. Therefore, this biomaterial system can be used for tissue engineering applications. Second, the brin/PEG-based sca olds were modi ed to be degradable via hydrolysis and to include bioactive ceramic particles (hydroxyapatite and -tri-calcium phosphate). Characteristics of the hydrogel ceramic composites were investigated in vitro and in vivo. The presence of ceramic particles extended degradation time of thehydrogels in vitro and in vivo. Hydrogel ceramic composites were tested in a rodent cranial defect model and enhanced bone tissue regeneration. Third, strategies developed from the previous studies were combined to prepare ceramic supplemented gradient sca olds for bone tissue engineering applications. A gradient layer was applied to the hydrogel-ceramic composites and bone tissue response was evaluated in a periosteum guided large animal model. Ceramic supplemented gradient sca olds augmented vascularization and bone regeneration in vivo. In conclusion, a biomaterial system with persistent growth factor gradients was developed and enhanced vascularization and bone regeneration in vivo. This system holds a great potential for tissue engineering applications.Ph.D. in Biomedical Engineering, December 201
IMAGING TISSUE SCAFFOLDS WITH X-RAY PHASE CONTRAST IMAGING
No full textA major challenge in tissue engineering is imaging within scaffolds. Biomaterials commonly used in tissue engineering have similar x-ray absorption properties to native tissue, so they provide poor contrast in radiography. X-ray phase contrast imaging (XPCI) is an imaging modality that measures light/matter interactions other than absorption. By providing insight into these interactions, x-ray phase contrast imaging has the potential to allow imaging of materials used in biomedical applications. In this thesis, a technique for imaging explanted poly(ethylene glycol) (PEG) hydrogels is presented. PEG is a highly biocompatible polymer with widespread use in biomedical applications. Porous PEG hydrogels were synthesized with 100-150 μm pore size through a salt-leaching technique and loaded with fibrin, a natural protein known to stimulate vascularized tissue formation. The hydrogels were formed in the shape of disks and implanted subcutaneously in the backs of rodent animal models for 1, 2 and 3 weeks. The hydrogels and surrounding tissue were harvested at 1, 2, and 3 weeks. After explanation, the hydrogels were placed in formaldehyde and imaged at the National Light Source at Brookhaven National Laboratory using a multiple image radiography (MIR) technique. Five hundred angles were captured of each sample over 180°, and computed tomography was performed. The samples were compared to histological stains to identify specific tissue features that could be identified in the XPCI images. XPCI allowed imaging of hydrogels and identification of interfaces between native tissue and the PEG material. In addition, tissue invasion into the pores of the scaffold could be identified and could be used to quantify the depth of invasion. Muscle tissue could also be seen, and within muscle fibers were visible. With computed tomography, 3D volumes were constructed, enabling analysis throughout the samples.M.S. in Biomedical Engineering, December 201
MULTIFUNCTIONAL BIOMATERIAL SYSTEM FOR DRUG DELIVERY AND SCAFFOLDING TO PROMOTE NEOVASCULARIZATION IN TISSUE ENGINEERING
No full textThe successful development of engineered tissues requires extensive vascular network formation. The overall goal of this work is to develop a multifunctional biomaterial system for scaffolding and drug delivery to promote neovascularization in engineered tissue. Firstly, a drug delivery system was developed for molecules of different properties. Poly(lactic-co-glycolic acid) (PLGA) was prepared into microspheres using a double emulsion process for delivery of hydrophobic chlorhexidine (CHX) and hydrophilic platelet-derived growth factor-BB (PDGF-BB). Both drugs exhibited bioactivity after release and the efficacy of dual drug delivery was evaluated with an infected wound animal model. The simultaneous delivery of CHX and PDGF-BB improved wound healing and neovascularization while reducing bacteria levels. Therefore, the PLGA microspheres can be used for long-term active delivery of both hydrophobic and hydrophilic molecules in tissue engineering applications. Secondly, a 3D scaffold was developed for tissue engineering applications. Poly(ethylene glycol) (PEG) hydrogels with interconnected pores were generated with a salt leaching technique. Fibrin was filled in the pores by adding fibrinogen solution to hydrogel scaffolds pre-loaded with thrombin. The hydrogels were evaluated in a rodent subcutaneous implant model, showing that tissue invasion with a higher vascular density occurred when the hydrogels were loaded with fibrin. This composite hydrogel supports vascularized tissue ingrowth, and thus holds potential for tissue engineering applications. Thirdly, approaches from the previous studies were combined to develop a multifunctional biomaterial system for tissue engineering scaffolding and sequential xi growth factor delivery. PLGA microspheres were incorporated into a fibrin loaded porous hydrogel, in which the PEG based scaffold was modified to allow controlled degradation via hydrolysis. Different growth factors were encapsulated in fibrin and PLGA microspheres to provide temporal control of delivery. Growth factors released with the appropriate sequence promoted stable and functional blood vessel formation. In conclusion, a multifunctional biomaterials system was developed to provide structural and mechanical support for tissue regeneration, as well as delivery of signals that stimulate neovascularization. The system holds great potential for tissue engineering applications. Future work will require the extensive collaboration from interdisciplinary fields towards the successful development of engineered tissue substitutes.PH.D in Biomedical Engineering, May 201
NEOVASCULARIZAnON WITHIN POROUS PEG HYDROGELS
No full textDevelopment of engineered tissues of clinically relevant size requires the ability to control vascularization within biomaterial scaffolds. Poly(ethylene glycol) (PEG) hydrogels have been extensively investigated for use as synthetic scaffolds to support engineered tissue formation. The goal of this work described was to develop techniques that can be used to enhance vascularized tissue formation in PEG-based hydrogels. In the first part of the study a technique was developed to generate porous PEG hydrogels using a salt leaching technique. This technique was then used to examine the role of pore size on vascularization and tissue remodeling in porous PEG hydrogel in vitro and in vitro. Both in vitro and in vivo studies showed that vessel invasion was pore size dependent. In addition, a thin layer of inflammatory tissue was observed between PEG hydrogel and blood vessels that formed within the gels. This layer suggested that inflammatory cells, not vascular cells, interacted with the surface of the material. This suggests that peptides covalently incorporated within PEG may not directly interact with endothelial cells (ECs) following implantation. The porous PEG hydrogels were very stable in vitro and in vivo and did not exhibit any signs of degradation. Hydrogels used in tissue engineering need to exhibit controlled degradation. In order to address the stability of PEG hydrogels, porous hydrogels were rendered using degradable PEG-co-(L-Lactic acid) diacrylate PEG-PLLA-DA. This polymer is degraded via hydrolysis of the PLLA chains. The porous PEG-PLLA-DA hydrogels were generated by solvent casting, photopolymerization, and particulate leaching. The influence of polymer conditions on the architecture, degradation, and mechanical properties of the hydrogels were investigated in vitro. The hydrogels were found to exhibit autofluorescence that allowed for the unique ability to nondestructively image hydrogel structure under fully swelled conditions using confocal microscopy. Initial pore size was a function of particulate size and independent of polymer concentration. Interestingly, pore size remained stable though out the study, and was not a function of degradation. In addition, degradation time of porous PEG-LLA-DA hydrogels was influenced by polymer concentration. Compressive modulus was a function of polymer concentration and pore size and decreased during hydrogel degradation. The incorporation of cell adhesion sequences into the hydrogel showed that they can support cell adhesion with morphology varying with pore size. This technique could be used to tailor porous biodegradable scaffolds for tissue engineering applications. In the final portion of this thesis a poly-lysine (PLL) molecule was synthesized in order to allow clustering of adhesion sequences in PEG hydrogels. Clusters of peptide sequences have been shown to enhance cell interactions with substrate surfaces. The sequence was synthesized and purified by high performance liquid chromatography (HPLC) and characterized by mass spectrometry. The side chains of the PLL molecule was used to attach peptide sequences. Cysteine contained within the PLL allowed incorporation into the PEG hydrogel by mixed mode polymerization. Cells were observed to adhere to hydrogels containing the RGD clusters and not to the control gels. The results presented here describe various techniques that can be used to optimize the design of polymer scaffolds for tissue engineering. In addition, the data provide insight into the process of vascularization in porous hydrogels and the influence of synthesis conditions and degradation on properties of porous hydrogels. Future studies should investigate the optimization of these material techniques for control of neovascularization within PEG hydrogels for tissue engineering applications.Ph.D. in Biomedical Engineering, December 201
ENGINEERING OF CLINICAL-SCALE, IN VITRO VASCULARIZED BONE TISSUE FOR IMPLANTATION
No full textTissue engineering has been a rapidly expanding field dedicated to regeneration of tissue. The field has focused on application through combinations of 3 key components: cells, signals, and scaffolds. One ambitious combination of all three is the desire to engineer functional tissues in vitro to meet the clinical-demand of organ replacement. While major advances have been made, a critical obstacle that has yet to be overcome is the need to grow large volumes of complex 3D tissue. In this proposal, this issue is addresed in two ways: the use of a perfusion bioreactor system to culture 3D scaffolds to enhance mass transport, and engineering of a vascular network withing the scaffold for rapid perfusion once implanted in vivo. This thesis aims to address both aspects for bone tissue engineering by engineering pre-vascularized, mineralizing scaffolds that can be scaled up to clinically-relevant volumes by using a tubular perfusion bioreactor system (TPS). To address this, 3 aims were addressed. First, 3D culture of endothelial colony forming cells (ECFCs), a clinically-relevant cell population, was demonstrated utilizing fibrin gels within the TPS. The TPS allowed for viable culture of ECFCs within fibrin bead scaffold up to 1 week without a reduction in cell amount or genomic quality of the cells. Second, a co-culture model of angiogenesis utilizing ECFCs and mesenchymal stem cells (MSCs) was demonstrated to reproducibly form pre-formed vessel networks within a mineralizing fibrin scaffold. Data shows that MSC suspension concentration and fibrinogen concentration modulate the angiogenic response. Mineralization is demonstrated without the use of osteogenic media utilizing shear stress within the TPS. Finally, functionality of the pre-formed vessels is demonstrated following implantation to a SCID mouse model. Engineered human vessels showed anastasmosis to the host vasculature, with evidence of interconnected host and human vessel networks as well as formation of hybrid vessels. Additionally, evidence of mineralization within the scaffolds is maintained in TPS-cultured samples. In demonstrating these aims, future work should focus on fortifying the scaffold material to enable addressing implantation and persistence of clinically-relevant tissue volumes. In conclusion, pre-vascularization within bioreactor-cultured scaffolds represents a promising solution for future tissue engineering application.Ph.D. in Biomedical Engineering, May 201
LGBTQIA+ Needs in Temporary Living Communities
No full textTemporary Living Communities (TLCs) are one of the biggest providers of housing for LGBTQIA+ (Lesbian, Gay, Bisexual, Transgender, Queer, Intersex, Asexual, plus additional identities not listed in this acronym) folk, with LGBTQIA+ youth being the most likely demographic to identify as homeless. For brevity and clarity, this paper will refer to the LGBTQIA+ population by the word “queer” (although this term may appear offensive to some, many queer individuals have reclaimed this term as a way to take power away from their oppressors by making the meaning positive instead of negative. I will be using the positive version of this term as well in my paper). Previous studies have estimated between 11 and 40 percent of all homeless youth identify as queer (Ventimiglia, 2012; Cochran, Stewart, & Ginzler, 2002). However, this number is hard to define due to the lack of a nationwide study (Whitbeck, Chen, Hoyt, Tyler, & Johnson, 2004) and because many disadvantaged queer youth do not disclose their identities because of the stigma of identifying as queer and possibly not wanting to risk being outed to their peers (Berberet, 2006). I want to investigate this topic deeper by examining how TLCs in the United States affect queer youth and if they adequately support their transition to being functional members in their communities.University of Wisconsin--Stout. Office of Research and Sponsored Program
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