Spelling suggestions: "subject:"solidstate hydrogen:deuterium exchange"" "subject:"solidstate hydrogenierter exchange""
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Effects of Formulation and Manufacturing Conditions on Protein Structure and Physical StabilityNathan E Wilson (7827434) 06 November 2019 (has links)
This work focuses on the effects of formulation and manufacturing as it effects protein structure and physical stability. Using common physical characterization techniques, X-ray photoelectron spectroscopy, and solid-state hydrogen/deuterium exchange with mass spectrometry, correlations are identified between these results and accelerated stability studies.
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SOLID-STATE HYDROGEN-DEUTERIUM EXCHANGE MASS SPECTROMETRY OF LYOPHILIZED PEPTIDESRajashekar Kammari (9095855) 08 July 2020 (has links)
<div>Proteins are susceptible to physical and chemical degradation in solution, which can lead to the loss of therapeutic activity and increase the potential for immunogenic responses when administered. Many degradation reactions are mediated by water, and therefore the proteins are often formulated as solids in which degradation rates are slowed significantly. Lyophilization is the most common method for producing solid protein formulations, which removes the water by sublimation and desorption under vacuum from the frozen protein solutions. Lyophilization requires excipients to protect the protein from the inherent stresses involved in the process. Degradation can still occur during lyophilization and storage, and needs to be characterized in order to develop a successful formulation with desired storage stability. The analytical techniques to characterize solid-state proteins are limited, however, and many do not provide site-specific information and lack the ability to predict stability beforehand.</div><div>Recently, solid-state hydrogen-deuterium exchange mass spectrometry (ssHDX-MS) has been developed to characterize proteins in solid powders with peptide level resolution. The technique was found to be sensitive to formulation and process changes. The ssHDX-MS metrics are highly correlated to the long-term storage stability, suggesting that the method can serve as a formulation screening tool. This dissertation aims to evaluate the factors affecting ssHDX kinetics and to develop a mechanistic understanding of the exchange process in solid samples, which in turn will support the solid-state protein development and enable it to be conducted in a more a cost and time-effective way. First, the contribution of peptide-matrix interactions to deuterium incorporation kinetics in the absence of higher-order structure was assessed using lyophilized poly-D, L-alanine peptides. Deuterium incorporation depended on excipient type and D<sub>2</sub>O<sub>(g)</sub> activity in the solid samples. A reversible pseudo-first-order kinetic model was proposed and validated using the experimental data. Second, the reversibility of the hydrogen-deuterium exchange reaction in the solid-state was evaluated to support the ssHDX mechanistic model further. The reaction was found to be reversible irrespective of initial conditions and independent of the excipient type. Pre-hydration of the peptide samples prior to deuterium labeling did not affect deuterium incorporation in amorphous samples compared to the controls not subjected to pre-hydration. Third, the contribution of peptide secondary structure to deuterium uptake kinetics was quantified using structured PDLA analogs. The deuterium incorporation in structured peptides was less than that of the PDLA peptides suggesting that both peptide structure and peptide-matrix interactions contribute to ssHDX-MS. Finally, a quantitative data analysis method was presented that allows the interpretation of ssHDX-MS data of a protein relative to controls. Altogether, the findings present a comprehensive mechanistic understanding of the ssHDX-MS of proteins that is relevant to the industry.</div>
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Solid-state Stability of Antibody-drug ConjugatesEunbi Cho (11192397) 28 July 2021 (has links)
<p>Antibody-drug conjugates (ADCs) combine
the cytotoxicity of traditional chemotherapy with the site-specificity of
antibodies by conjugating payloads to antibodies with immunoaffinity. However,
the conjugation alters the physicochemical properties of antibodies, increasing
the risks of various types of degradation. The effects of common risk factors
such as pH, temperature, and light on the stability of ADCs differ from their
effects on monoclonal antibodies (mAb) due to these altered physicochemical
properties. </p>
<p>To date, ADC researchers have
developed linkers with improved <i>in vivo</i> stability, and begun to
understand the deconjugation mechanisms <i>in vivo</i>. In contrast, the <i>in
vitro</i> stability of ADCs has not gained comparable attention. All nine of
the U.S. FDA approved ADCs are lyophilized to minimize the potential for
degradation. However, there are few studies on the solid-state stability of
ADCs. To evaluate lyophilized solids, pharmaceutical development relies heavily
on accelerated stability studies, which take months to determine the best formulation.
Characterization methods that are often used orthogonally with accelerated
studies include Fourier-transform infrared spectroscopy (FT-IR), Raman
spectroscopy, near-infrared spectroscopy (NIR), differential scanning
calorimetry (DSC), and x-ray powder diffraction (XRPD). Results from these methods are often poorly
correlated with stability, however. Thus, stability evaluation of solid-state ADC
products, and other recombinant protein drugs, is often a bottleneck in their
development.</p>
<p>To provide knowledge on how to
improve the <i>in vitro</i> stability of lyophilized ADC formulations, the solid-state
stability of ADC formulations with varying risk factors was studied in this
dissertation project. The first study investigated interactions between an ADC
and excipients in terms of solid-state stability enhancement. The second study
investigated the process-driven instability of ADCs during lyophilization using
various concentrations of ADCs. The first two studies incorporate a new method
called solid-state hydrogen/deuterium exchange coupled with mass spectrometry
(ssHDX-MS) as an analytical predictor of solid-state stability. The last study
investigated the effects of pH on the stability of labile hydrazones, as a
model for common linker chemistry used in ADCs. </p>
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