SONOPHORESIS .1. THE USE OF HIGH-FREQUENCY ULTRASOUND TO ENHANCE TRANSDERMAL DRUG DELIVERY

被引:112
作者
BOMMANNAN, D
OKUYAMA, H
STAUFFER, P
GUY, RH
机构
[1] UNIV CALIF SAN FRANCISCO,SCH PHARM,DEPT PHARM,SAN FRANCISCO,CA 94143
[2] SS PHARMACEUT CO LTD,TOKYO,JAPAN
[3] UNIV CALIF SAN FRANCISCO,DEPT PHARMACEUT CHEM,SAN FRANCISCO,CA 94143
[4] UNIV CALIF SAN FRANCISCO,DEPT RADIAT ONCOL,SAN FRANCISCO,CA 94143
[5] UNIV CALIF BERKELEY,GRAD GRP BIOENGN,BERKELEY,CA 94720
关键词
SONOPHORESIS; ULTRASOUND; TRANSDERMAL DELIVERY; SALICYLIC ACID; STRATUM-CORNEUM;
D O I
10.1023/A:1015808917491
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Previous attempts to use ultrasound (less-than-or-equal-to 1-MHz frequency and 1 to 3-W/cm2 intensity) to enhance transdermal drug delivery (so-called sonophoresis) have produced inconsistent results. Theoretical analysis of ultrasound propagation in tissue predicts that higher-frequency ultrasound (> 1 MHz) will increase the concentration of energy deposition in the stratum corneum (SC) (typically, the rate-limiting barrier to percutaneous penetration). This hypothesis was tested by comparing the passive transdermal delivery of salicylic acid with that under the influence of ultrasound at 2-, 10-, and 16-MHz frequency; measurements were performed in vivo in hairless guinea pigs. Total drug absorbed was quantified by determining the amount of salicylic acid (1) present in SC tape strips and (2) eliminated in urine. Sonophoresis for 20 min at 2 MHz caused no significant increase in salicylic acid delivery over passive diffusion; treatment with ultrasound at 10 and 16 MHz, on the other hand, significantly elevated salicylic acid transport, by 4-fold and 2.5-fold, respectively. Kinetic analysis of the sonophoretic data at 10 and 16 MHz also revealed that the diffusion lag time associated with transdermal drug delivery (TDD) was reduced. A shorter period (5 min) of sonophoresis again resulted in enhanced TDD (relative to the corresponding control) at the higher frequencies; the delivered dose, and the level of enhancement, however, were lower than those after the 20-min treatment. In a separate series of experiments, it was shown that (a) ultrasound did not alter the release kinetics of salicylic acid from the gel formulation used and (b) pretreatment of the skin with ultrasound at 10 and 16 MHz lowered skin barrier function such that the subsequent delivery of salicylic acid was enhanced compared to passive transport without sonophoresis pretreatment. It follows that the enhancing effect of sonophoresis is due to a direct effect of ultrasound on (presumably) the stratum corneum.
引用
收藏
页码:559 / 564
页数:6
相关论文
共 31 条
[1]   IONTOPHORETIC DRUG DELIVERY - EFFECTS OF PHYSICOCHEMICAL FACTORS ON THE SKIN UPTAKE OF NONPEPTIDE DRUGS [J].
BEHL, CR ;
KUMAR, S ;
MALICK, AW ;
DELTERZO, S ;
HIGUCHI, WI ;
NASH, RA .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1989, 78 (05) :355-360
[2]   USE OF ULTRASOUND TO ENHANCE PERCUTANEOUS-ABSORPTION OF BENZYDAMINE [J].
BENSON, HAE ;
MCELNAY, JC ;
HARLAND, R .
PHYSICAL THERAPY, 1989, 69 (02) :113-118
[3]   INVIVO AND INVITRO RELEASE OF MACROMOLECULES FROM POLYMERIC DRUG DELIVERY SYSTEMS [J].
BROWN, LR ;
WEI, CL ;
LANGER, R .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1983, 72 (10) :1181-1185
[4]   CHARACTERIZATION OF THE PORE TRANSPORT-PROPERTIES AND TISSUE ALTERATION OF EXCISED HUMAN-SKIN DURING IONTOPHORESIS [J].
BURNETTE, RR ;
ONGPIPATTANAKUL, B .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1988, 77 (02) :132-137
[5]  
BURNETTE RR, 1989, TRANSDERMAL DRUG DEL, P247
[6]  
CARSON P L, 1978, Ultrasound in Medicine and Biology, V3, P341, DOI 10.1016/0301-5629(78)90076-5
[7]   DIRECT-CURRENT IONTOPHORETIC TRANSDERMAL DELIVERY OF PEPTIDE AND PROTEIN DRUGS [J].
CHIEN, YW ;
SIDDIQUI, O ;
SHI, WM ;
LELAWONGS, P ;
LIU, JC .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1989, 78 (05) :376-383
[8]   DISTRIBUTION AND DEPOSITION OF TRITIATED CORTISOL USING PHONOPHORESIS [J].
DAVICK, JP ;
MARTIN, RK ;
ALBRIGHT, JP .
PHYSICAL THERAPY, 1988, 68 (11) :1672-1675
[9]  
ELIAS PM, 1983, J INVEST DERMATOL, V80, pS44, DOI 10.1038/jid.1983.12
[10]  
FELLINGER K, 1956, KLINIK THERAPIE CHRO, P549