Publications by authors named "Jeremiah Moore"

We present a new integrated experimental and modeling effort that assesses the intrinsic sensitivity of energetic materials based on their reaction rates. The High Explosive Initiation Time (HEIT) experiment has been developed to provide a rapid assessment of the high-temperature reaction kinetics for the chemical decomposition of explosive materials. This effort is supported theoretically by quantum molecular dynamics (QMD) simulations that depict how different explosives can have vastly different adiabatic induction times at the same temperature.

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There are few techniques available for chemists to obtain time-to-explosion data with known temperature inputs at the early stages of the design and synthesis of new explosives. In the 1960s, a technique was developed to rapidly heat milligram-quantities of confined explosives to ∼1000 K on microsecond timescales. Wenograd [Trans.

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Article Synopsis
  • Lymphoma treatment, particularly with Bruton tyrosine kinase inhibitors (BTKi), significantly increases the risk of developing new-onset atrial fibrillation (AF) compared to other treatments or no treatment.
  • In a study with nearly 2,000 lymphoma patients, the 5-year rate of AF was found to be 25% for those on BTKi, compared to only 8% for non-BTKi treatments and 4% for untreated patients.
  • Additionally, new cases of AF were linked to higher mortality risk, highlighting the importance of monitoring for AF in lymphoma patients, especially those with additional risk factors like older age and hypertension.
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Monoclonal antibody induced infusion reactions (IRs) can be serious and even fatal. We used clinical data and blood samples from 37 treatment naïve patients with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL) initiating therapy for progressive disease with a single 50 mg dose of intravenous (IV) rituximab at 25 mg/h. Twenty-four (65 %) patients had IRs at a median of 78 min (range 35-128) and rituximab dose of 32 mg (range 15-50).

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  • This study investigates the risk of arrhythmias in patients being treated for lymphoma, focusing on a large cohort of 2064 patients from the University of Rochester Medical Center Lymphoma Database.
  • The findings indicate that patients treated with Bruton tyrosine kinase inhibitors (BTKi), especially ibrutinib, had a significantly higher risk of developing arrhythmias (61%) compared to those who received no treatment (18%), with atrial fibrillation/flutter being the most common type.
  • The research suggests that individuals undergoing lymphoma treatment should be closely monitored for heart-related issues, particularly those who have no prior history of arrhythmias, as they are at an increased risk of developing cardiotoxicity during their treatment.
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Most patients with treatment naïve classical hairy cell leukemia (cHCL) have durable responses with purine nucleoside analogues. In contrast, options are limited for cHCL patients with co-morbidities, purine analogue intolerance, or resistant disease. We report the utility of targeted therapy for nine cHCL patients presenting with treatment naïve cHCL and severe neutropenia and infection (n = 3), purine analogue intolerance (n = 2), or purine analogue resistant disease (n = 4).

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Background: As oral targeted agents, such as ibrutinib, become more widely used, understanding the impact of suboptimal dosing on overall survival (OS) and progression-free survival (PFS) outside of clinical trials is imperative.

Patients And Methods: Data on ibrutinib discontinuation, dose reductions, and treatment interruptions were collected on 170 non-Hodgkin lymphoma and chronic lymphocytic leukemia (CLL; n = 115, 64%) patients treated with ibrutinib at a single institution. Ibrutinib dose adherence was calculated as the proportion of days in which ibrutinib was administered out of the total number of days ibrutinib was prescribed in the first 8 weeks.

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A pH-responsive, luminescent, dimetallic Eu(III)-containing complex has been synthesized and exhibits a unique mechanism of response. The luminescence-decay rate of the complex is slow, due to a lack of water molecules coordinated to the Eu(III) ions. However, the luminescence-decay rate decreases with increasing pH over a biologically relevant range of 4-8.

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Molecules containing multiple lanthanide ions have unique potential in applications for medical imaging including the areas of magnetic resonance imaging (MRI) and fluoresence imaging. The study of multilanthanide complexes as contrast agents for MRI and as biologically responsive fluorescent probes has resulted in an improved understanding of the structural characteristics that govern the behavior of these complexes. This review will survey the last five years of progress in multinuclear lanthanide complexes with a specific focus on the structural parameters that impact potential medical imaging applications.

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