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1 delivery of therapeutic RNAs to the lung via nebulization.
2 introduced into the gas phase by nanodroplet nebulization.
3 y mAb in foals for at least 5 days following nebulization.
4 pectra of water droplets formed by pneumatic nebulization.
5 th opposite polarities produced by pneumatic nebulization.
6 of the virus were then measured 15 min post nebulization.
7 -fold enhancement over conventional solution nebulization.
8 tains structural integrity and potency after nebulization.
9 nt to materials synthesis are cavitation and nebulization.
10 rded respirable-size aerosol particles after nebulization.
11 radical cations are produced with pneumatic nebulization.
12 cing more sample into the plasma compared to nebulization.
13 ed with an accuracy of 91.7 % using solution nebulization.
14 ed with ZIP-lipids (ZIP-LNPs) were stable to nebulization across a wide range of formulation paramete
16 ing fluid (ELF) and plasma after aerosolized nebulization (AeroEclipse), of amphotericin B lipid comp
20 the combination of pulmonary delivery using nebulization and external light activation has been show
21 0.5% to 37.4 +/- 1.6%, with breath-actuated nebulization and humidity identified as the most importa
22 in acetonitrile microdroplets generated via nebulization and measured by mass spectrometry of the co
23 unique challenges including stability during nebulization and penetration through both cellular and e
24 ll RNA delivery into the murine lung through nebulization and presents a potential sEV-based therapeu
25 inephrine infusion, and continuous albuterol nebulization) and respiratory compromise requiring mecha
26 ion buffer to increase the LNP charge during nebulization, and by the addition of a branched polymeri
28 ametric optimization of sample introduction, nebulization, and hollow cathode source conditions is pe
29 ts, due to the thermal treatment inherent to nebulization, and thus avoids salt-adduct formation that
31 lization-induced aggregation by altering the nebulization buffer to increase the LNP charge during ne
32 idic dialysis buffer, and excipient-assisted nebulization buffer, demonstrates exceptional stability
33 analysis with greater sensitivity than with nebulization by eliminating the dilution inherent to dis
35 eriments with enzymic proteins revealed that nebulization caused no detectable loss of catalytic acti
36 Therefore, appropriate modifications in the nebulization chamber and in the conventional nebulizer w
38 metric optimization for sample introduction, nebulization, desolvation, and hollow cathode source con
43 bles affecting the extraction yield were the nebulization gas flow rate, liquid flow rate, extraction
45 Compared to commercial ESI sources using nebulization gas to reduce discharge, 10-100-fold enhanc
47 cated to a) sham group, b) saline continuous nebulization group, c) 20 mg of albuterol continuous neb
48 tion group, c) 20 mg of albuterol continuous nebulization group, or d) 40 mg of albuterol continuous
49 e biodistribution given intravenously or via nebulization has not been extensively studied, though pr
51 CPMS methodology over conventional pneumatic nebulization-ICP(MS)/MS, the results of which were serio
54 ility for over 90 days and ensures efficient nebulization in preclinical male mouse, pup rat, and mal
55 ed by losartan at concentrations achieved by nebulization in the airway and oral application in the b
57 LNP formulations can be stabilized to resist nebulization-induced aggregation by altering the nebuliz
61 impaction, followed by analysis by solution nebulization MC-ICP-MS, as well as imaging using electro
62 y in mice, supporting an application of this nebulization methodology to deliver functional small RNA
63 lative softness of these CD-coupled acoustic nebulization methods in comparison to that of ESI using
65 lets with respiratory distress syndrome, the nebulization of 400 mg/kg of poractant alfa using a cust
66 HELIOX or AIR as the driving gas for updraft nebulization of a mixture of albuterol 2.5 mg and ipratr
68 Laboratory NH(4)(+) were generated from the nebulization of ammonium salt solutions and collected us
69 lude that administration through aerosolized nebulization of amphotericin B lipid complex every 24 hr
70 e of HELIOX as a driving gas for the updraft nebulization of bronchodilators during the first 2 hrs o
71 mass concentrations generated by ultrasonic nebulization of deionized (DI) water stored in a variety
77 n SMCs or pharmacological Rac1 inhibition by nebulization of NSC23766 prevented AHR in murine models
78 atment includes airway clearance techniques; nebulization of saline to loosen tenacious secretions; a
80 the clinical potential of CXCR7 antagonism, nebulization of the agent before and after the inflammat
81 ly technique has been developed that entails nebulization of the compound dissolved in ethanol and su
82 aerosol-phase extraction (APE), is based on nebulization of the extracting aqueous solution (0.1 mol
84 er inhalation injury and identifies low-dose nebulization of tiotropium bromide as a potentially effi
90 ivery of nitrite dissolved in saline through nebulization produced selective, sustained pulmonary vas
91 mide 1 hr before injury (n=6) and postinjury nebulization protocols of 18 mug (n=6), 36 mug (n=6), an
94 entional sample introduction using pneumatic nebulization requires the dissolution of these samples,
95 re aminoglycosides (RR, 0.67 [0.47-0.97]) or nebulization (RR, 0.64 [0.49-0.83]) were used as opposed
96 S for a range of mineral waters by pneumatic nebulization sample introduction and the analysis of gen
97 metry (MS) detection, demonstrating that SAW nebulization (SAWN) can be performed either in a discont
98 arge (CD) coupled to a surface acoustic wave nebulization (SAWN) device enhanced sampling performance
99 erformance for APCI, a surface acoustic wave nebulization (SAWN) device was implemented to convert li
102 the energy used for the formation (i.e., by nebulization, sonication, or electrospray) of these syst
103 nd, we developed and characterized a tunable nebulization system composed of an ultrasonic transducer
106 Two major findings are realized for three nebulization systems: (1) a direct injection high-effici
107 report the optimization and use of SAWN as a nebulization technique for the introduction of samples f
108 ory group compared 6 protocols: 4 followed a nebulization technique using hypertonic saline, and 2 fo
111 tainty regarding the integrity of sEVs after nebulization, the delivery efficiency of aerosolized sEV
117 stered through the airway (intranasal or via nebulization) versus the systemic route (intraperitoneal
118 was reduced to 540 mg, and the frequency of nebulization was increased to 5/6 time points (0, 12, 24
121 omparison of the response to direct solution nebulization when using a sample flow rate of 2 mL min(-
123 of their constituent lipids by employing SAW nebulization with corona discharge (CD) ionization.
124 ated with the TLR2 agonist Pam3CSK4 prior to nebulization with the neutrophil chemotactic agent LTB4.
126 are generated by atomizing bulk water using nebulization without the application of an external elec
127 d that albuterol administered via continuous nebulization would mitigate acute lung injury after smok