ULTRASONIC NEBULIZATION OF HYPERTONIC SOLUTION - A NEW METHOD FOR OBTAINING SPECIMENS FROM NASAL-MUCOSA FOR MORPHOLOGIC AND BIOCHEMICAL-ANALYSIS IN ALLERGIC RHINITIS
G. Melillo et al., ULTRASONIC NEBULIZATION OF HYPERTONIC SOLUTION - A NEW METHOD FOR OBTAINING SPECIMENS FROM NASAL-MUCOSA FOR MORPHOLOGIC AND BIOCHEMICAL-ANALYSIS IN ALLERGIC RHINITIS, Allergy, 53(8), 1998, pp. 794-797
Various techniques are used to collect specimens from the nasal mucosa
for morphologic and biochemical analysis. The purpose of this study w
as to devise a method that overcomes some of the disadvantages (e.g.,
invasive procedure, samples not suitable for cytologic and biochemical
analysis, lack of standardization, and poor reproducibility) of these
techniques. The new method requires subjects, with neck extended, to
inhale an ultrasonic nebulization of a hypertonic (3% NaCl) solution (
UNHS) for 5 min. They then blow their nose into a Petri dish, one nost
ril at a time with the other one blocked. The secretions are dispersed
with 0.1% dithiothreitol in phosphate buffer solution for 20 min. Tot
al cell count (TCC) is evaluated, and the cellular suspension is divid
ed into two aliquots: one is centrifuged and the supernatants are coll
ected for eosinophil cationic protein (ECP) measurements; the other is
cytocentrifuged and the slides, stained with Diff-Quik, are used for
differential cell count. The results obtained with the UNHS and nasal
lavage (NL) methods were compared. Eleven nonatopic healthy subjects a
nd 19 allergic rhinitic patients were studied. Total cell count (x10(5
)) was significantly higher with UNHS than with NL (13.0+/-12.3 vs 1.9
+/-1.6; P<0.01) The differential cell count was similar with the two p
rocedures. ECP levels (mu g/l) were higher with UNHS than with NL (39.
1+/-38.2 vs 16.7+/-41.2; P<0.01). For evaluation of reproducibility, f
our healthy and six rhinitic subjects underwent UNHS on two occasions
within 5 days, and the results of two samples (sample 1 vs sample 2) w
ere analyzed. Reproducibility was good as to TCC, differential cell co
unt, and ECP.