Abstract:The 21st Congress for the International Society for Aerosols in Medicine included, for the first time, a session on Pulmonary Delivery of Therapeutic and Diagnostic Gases. The rationale for such a session within ISAM is that the pulmonary delivery of gaseous drugs in many cases targets the same therapeutic areas as aerosol drug delivery, and is in many scientific and technical aspects similar to aerosol drug delivery. This article serves as a report on the recent ISAM congress session providing a synopsis of e… Show more
“…The technique is, in general, versatile and different acquisition compromises are possible, each optimal for different applications. For example, in a study of dynamic recovery from an asthma event 25 , SVI data was analyzed at a higher temporal resolution (~7 min vs. ~18 min) and the same spatial resolution, at the cost of a ~ 30% increase in uncertainty of specific ventilation (estimated from Monte Carlo simulations). A recent modeling study 26 sought to quantify the impact of several minor limitations of the SVI technique, namely 1) that the imaged volume does not encompass the entire right lung, 2) that small misalignments between successive images may exist even after registration, and 3) that pulmonary veins, by transporting blood from elsewhere in the lung into an imaged region, may add confounding signal that reflects ventilation in the region where that blood was originally oxygenated and not in the region in which it is being imaged.…”
Specific ventilation imaging (SVI) is a functional magnetic resonance imaging technique capable of quantifying specific ventilationthe ratio of the fresh gas entering a lung region divided by the region's end-expiratory volumein the human lung, using only inhaled oxygen as a contrast agent. Regional quantification of specific ventilation has the potential to help identify areas of pathologic lung function. Oxygen in solution in tissue shortens the tissue's longitudinal relaxation time (T 1 ), and thus a change in tissue oxygenation can be detected as a change in T 1 -weighted signal with an inversion recovery acquired image. Following an abrupt change between two concentrations of inspired oxygen, the rate at which lung tissue within a voxel equilibrates to a new steady-state reflects the rate at which resident gas is being replaced by inhaled gas. This rate is determined by specific ventilation. To elicit this sudden change in oxygenation, subjects alternately breathe 20-breath blocks of air (21% oxygen) and 100% oxygen while in the MRI scanner. A stepwise change in inspired oxygen fraction is achieved through use of a custom threedimensional (3D)-printed flow bypass system with a manual switch during a short end-expiratory breath hold. To detect the corresponding change in T 1 , a global inversion pulse followed by a single shot fast spin echo sequence was used to acquire two-dimensional T 1 -weighted images in a 1.5 T MRI scanner, using an eight-element torso coil. Both single slice and multi-slice imaging are possible, with slightly different imaging parameters. Quantification of specific ventilation is achieved by correlating the time-course of signal intensity for each lung voxel with a library of simulated responses to the air/oxygen stimulus. SVI estimations of specific ventilation heterogeneity have been validated against multiple breath washout and proved to accurately determine the heterogeneity of the specific ventilation distribution.
“…The technique is, in general, versatile and different acquisition compromises are possible, each optimal for different applications. For example, in a study of dynamic recovery from an asthma event 25 , SVI data was analyzed at a higher temporal resolution (~7 min vs. ~18 min) and the same spatial resolution, at the cost of a ~ 30% increase in uncertainty of specific ventilation (estimated from Monte Carlo simulations). A recent modeling study 26 sought to quantify the impact of several minor limitations of the SVI technique, namely 1) that the imaged volume does not encompass the entire right lung, 2) that small misalignments between successive images may exist even after registration, and 3) that pulmonary veins, by transporting blood from elsewhere in the lung into an imaged region, may add confounding signal that reflects ventilation in the region where that blood was originally oxygenated and not in the region in which it is being imaged.…”
Specific ventilation imaging (SVI) is a functional magnetic resonance imaging technique capable of quantifying specific ventilationthe ratio of the fresh gas entering a lung region divided by the region's end-expiratory volumein the human lung, using only inhaled oxygen as a contrast agent. Regional quantification of specific ventilation has the potential to help identify areas of pathologic lung function. Oxygen in solution in tissue shortens the tissue's longitudinal relaxation time (T 1 ), and thus a change in tissue oxygenation can be detected as a change in T 1 -weighted signal with an inversion recovery acquired image. Following an abrupt change between two concentrations of inspired oxygen, the rate at which lung tissue within a voxel equilibrates to a new steady-state reflects the rate at which resident gas is being replaced by inhaled gas. This rate is determined by specific ventilation. To elicit this sudden change in oxygenation, subjects alternately breathe 20-breath blocks of air (21% oxygen) and 100% oxygen while in the MRI scanner. A stepwise change in inspired oxygen fraction is achieved through use of a custom threedimensional (3D)-printed flow bypass system with a manual switch during a short end-expiratory breath hold. To detect the corresponding change in T 1 , a global inversion pulse followed by a single shot fast spin echo sequence was used to acquire two-dimensional T 1 -weighted images in a 1.5 T MRI scanner, using an eight-element torso coil. Both single slice and multi-slice imaging are possible, with slightly different imaging parameters. Quantification of specific ventilation is achieved by correlating the time-course of signal intensity for each lung voxel with a library of simulated responses to the air/oxygen stimulus. SVI estimations of specific ventilation heterogeneity have been validated against multiple breath washout and proved to accurately determine the heterogeneity of the specific ventilation distribution.
“…NO, O 2 , CO, H 2 S, Xe) to elicit beneficial biological responses for disease treatment is gaining popularity in recent years. 112 For example, nitric oxide (NO) plays important roles in human biology, such as being neurotransmitters and neuromodulators in the human central nervous system, [113][114][115] and is now accepted as a treatment for pulmonary hypertension due to its ability to relax vascular smooth muscle. 116 Like NO, carbon monoxide (CO) is a gasotransmitter, as well as possessing antiinflammatory and anti-apoptotic properties.…”
Section: Can Allow Design Of Specific Mof-hydrogel Composites Targete...mentioning
Metal organic frameworks (MOFs) are incredibly versatile three-dimensional porous materials with a wide range of applications that arise from their well-defined coordination structures, high surface areas and porosities, as well...
“…1 Inhaled NO is approved by the US Food and Drug Administration for use in persistent pulmonary hypertension of the newborn, but commonly is used off label in critically ill adult patients worldwide to reduce increased pulmonary vascular resistance (PVR) for afterload reduction during acute right-sided heart failure (RHF) 2 or to treat hypoxic pulmonary vasoconstriction. 2,3 These indications are most common in the subset of adult patients undergoing cardiovascular or thoracic surgery. The agent is initiated either in the operating room or in the intensive care unit (ICU) before or after surgery.…”
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