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1.
Int J Pharm ; 637: 122887, 2023 Apr 25.
Article in English | MEDLINE | ID: mdl-36990171

ABSTRACT

This manuscript systematically assesses three different glycerides (tripalmitin, glyceryl monostearate, and a blend of mono-, di- and triesters of palmitic and stearic acids (Geleol™)) as potential gelator structuring agents of medium-chain triglyceride oil to form an oleogel-based injectable long-acting local anesthetic formulation for postoperative pain management. Drug release testing, oil-binding capacity, injection forces, x-ray diffraction, differential scanning calorimetry, and rheological testing were serially performed to characterize the functional properties of each oleogel. After benchtop assessment, the superior bupivacaine-loaded oleogel formulation was compared to bupivacaine HCl, liposomal bupivacaine, and bupivacaine-loaded medium-chain triglyceride oil in a rat sciatic nerve block model to assess in vivo long-acting local anesthetic performance. In vitro drug release kinetics were similar for all formulations, indicating that drug release rate is primarily dependent on the drug's affinity to the base oil. Glyceryl monostearate-based formulations had superior shelf-life and thermal stability. The glyceryl monostearate oleogel formulation was selected for in vivo evaluation. It was found to have a significantly longer duration of anesthetic effect than liposomal bupivacaine and was able to provide anesthesia twice as long as the equipotent bupivacaine-loaded medium-chain triglyceride oil, indicating that the increased viscosity of the oleogel provided enhanced controlled release over the drug-loaded oil alone.


Subject(s)
Anesthetics, Local , Bupivacaine , Rats , Animals , Glycerides/chemistry , Triglycerides
2.
Langmuir ; 37(42): 12419-12428, 2021 Oct 26.
Article in English | MEDLINE | ID: mdl-34644078

ABSTRACT

Nanosphere lithography employs single- or multilayer self-assembled nanospheres as a template for bottom-up nanoscale patterning. The ability to produce self-assembled nanospheres with minimal packing defects over large areas is critical to advancing applications of nanosphere lithography. Spin coating is a simple-to-execute, high-throughput method of nanosphere self-assembly. The wide range of possible process parameters for nanosphere spin coating, however-and the sensitivity of nanosphere self-assembly to these parameters-can lead to highly variable outcomes in nanosphere configuration by this method. Finding the optimum process parameters for nanosphere spin coating remains challenging. This work adopts a design-of-experiments approach to investigate the effects of seven factors-nanosphere wt%, methanol/water ratio, solution volume, wetting time, spin time, maximum revolutions per minute, and ramp rate-on two response variables-percentage hexagonal close packing and macroscale coverage of nanospheres. Single-response and multiple-response linear regression models identify main and two-way interaction effects of statistical significance to the outcomes of both response variables and enable prediction of optimized settings. The results indicate a tradeoff between the high ramp rates required for large macroscale coverage and the need to minimize high shear forces and evaporation rates to ensure that nanospheres properly self-assemble into hexagonally packed arrays.

3.
Anal Bioanal Chem ; 413(1): 49-71, 2021 Jan.
Article in English | MEDLINE | ID: mdl-33073312

ABSTRACT

The unprecedented global pandemic known as SARS-CoV-2 has exercised to its limits nearly all aspects of modern viral diagnostics. In doing so, it has illuminated both the advantages and limitations of current technologies. Tremendous effort has been put forth to expand our capacity to diagnose this deadly virus. In this work, we put forth key observations in the functionality of current methods for SARS-CoV-2 diagnostic testing. These methods include nucleic acid amplification-, CRISPR-, sequencing-, antigen-, and antibody-based detection methods. Additionally, we include analysis of equally critical aspects of COVID-19 diagnostics, including sample collection and preparation, testing models, and commercial response. We emphasize the integrated nature of assays, wherein issues in sample collection and preparation could impact the overall performance in a clinical setting.


Subject(s)
COVID-19/diagnosis , Molecular Diagnostic Techniques/methods , Pandemics , SARS-CoV-2/isolation & purification , COVID-19/virology , Clustered Regularly Interspaced Short Palindromic Repeats , Humans , RNA, Viral/analysis , SARS-CoV-2/genetics , Specimen Handling/methods
4.
Biosens Bioelectron ; 135: 137-144, 2019 Jun 15.
Article in English | MEDLINE | ID: mdl-31005765

ABSTRACT

Foodborne illnesses are a major contributor to misery and health challenges in both rich and poor nations. Illnesses from pathogens such as Escherichia coli and Cryptosporidium parvum oocysts account for most of the cases of diarrhea in the world. Many standard methods exist for detecting these pathogens in water. However, these standard methods do not readily translate to the detection of the same pathogens in food. Detection techniques for pathogens in food are often inadequate, due to their inability to completely separate pathogens from food matrices. In this paper, we present a technique to separate and detect both Escherichia coli cells and Cryptosporidium parvum oocysts that have been embedded in ground meat. We achieve this objective by combining enzymatic digestion of the meat, hydrodynamic cavitation to disassemble pathogens from the meat, immunomagnetic separation to purify meat samples and indirect electrochemical detection of the target pathogens. Our use of hydrodynamic cavitation to separate pathogens is compared against an industry standard separation technique. Results indicate that the use of hydrodynamic cavitation amplifies the detection capabilities of our sensing technique and is overall comparable to or better than conventional stomacher sample preparation.


Subject(s)
Cryptosporidium parvum/isolation & purification , Escherichia coli O157/isolation & purification , Food Analysis/methods , Red Meat/microbiology , Animals , Biosensing Techniques/economics , Biosensing Techniques/methods , Cattle , Cryptosporidiosis/diagnosis , Cryptosporidiosis/microbiology , Escherichia coli Infections/diagnosis , Escherichia coli Infections/microbiology , Food Analysis/economics , Food Contamination/analysis , Foodborne Diseases/diagnosis , Foodborne Diseases/microbiology , Hydrodynamics , Immunomagnetic Separation/economics , Immunomagnetic Separation/methods , Time Factors
5.
Sensors (Basel) ; 18(5)2018 May 10.
Article in English | MEDLINE | ID: mdl-29747467

ABSTRACT

The availability of clean drinking water is a significant problem worldwide. Many technologies exist for purifying drinking water, however, many of these methods require chemicals or use simple methods, such as boiling and filtering, which may or may not be effective in removing waterborne pathogens. Present methods for detecting pathogens in point-of-use (POU) sterilized water are typically time prohibitive or have limited ability differentiating between active and inactive cells. This work describes a rapid electrochemical sensor to differentially detect the presence of active Escherichia coli (E. coli) O157:H7 in samples that have been partially or completely sterilized using a new POU electrocatalytic water purification technology based on superradicals generated by defect laden titania (TiO2) nanotubes. The sensor was also used to detect pathogens sterilized by UV-C radiation for a comparison of different modes of cell death. The sensor utilizes immunomagnetic bead separation to isolate active bacteria by forming a sandwich assay comprised of antibody functionalized secondary magnetic beads, E. coli O157:H7, and polyguanine (polyG) oligonucleotide functionalized secondary polystyrene beads as an electrochemical tag. The assay is formed by the attachment of antibodies to active receptors on the membrane of E. coli, allowing the sensor to differentially detect viable cells. Ultravioloet (UV)-C radiation and an electrocatalytic reactor (ER) with integrated defect-laden titania nanotubes were used to examine the sensors’ performance in detecting sterilized cells under different modes of cell death. Plate counts and flow cytometry were used to quantify disinfection efficacy and cell damage. It was found that the ER treatments shredded the bacteria into multiple fragments, while UV-C treatments inactivated the bacteria but left the cell membrane mostly intact.

6.
Environ Entomol ; 47(2): 477-483, 2018 04 05.
Article in English | MEDLINE | ID: mdl-29462264

ABSTRACT

We examined the effects of humidity on the metabolic rates and respiratory patterns of Gromphadorhina portentosa (Schaum) (Blattodea: Blaberidae) to determine whether insects transition from continuous, cyclical, and discontinuous (DGC) respiration in response to water conservation. Eight male G. portentosa were placed under five different humidity treatments (0, 23, 40, 60, 80% RH). Using flow through respirometry we: (i) determined the effect of humidity on metabolic rate; (ii) observed if changes in metabolic rate were correlated with changes in closed/flutter (CF) or the open (O) phase of DGC; and (iii) determined whether increased spiracular closure was correlated with an increase in water retention. Although G. portentosa had similar rates of CO2 release when placed under 0, 40, 60, and 80% RH, cockroaches placed at 23% RH had a significantly higher metabolic rate. There was no effect of humidity on the duration of the CF phase of the DGC. However, the O phase of DGC was significantly longer when G. portentosa was placed at humidity levels above 23% RH. Interestingly, we saw that the average rate of mass lost to the environment did not change when cockroaches were placed at humidity levels ranging from 0 to 80% RH. This suggests that modulation of the spiracles allows G. portentosa to regulate the amount of water lost to the environment.


Subject(s)
Basal Metabolism , Cockroaches/metabolism , Water/physiology , Animals , Cell Respiration , Humidity , Male
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