Sonophoresis
Sonophoresis
Sonophoresis
Hiren Patel
M.PHARM E mail- [email protected] APMC College of Pharmaceutical Edu. & Res. Himatnagar
Contents
1. Introduction 2. Sonophoresis: a historical perspective 3. Generation of ultrasound 4. Biological effect of ultrasound 5. Mechanism of sonophoresis 6. Synergetic effect with other enhancers 7. Safety 8. Applications of sonophoresis 9. Advantages 10. Limitations 11. Drugs used by sonophoretic drug delivery 12. Conclusion 13. References
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1. Introduction
Definition: sonophoresis is the enhancement of
migration of drug molecules through the skin by ultrasonic energy Sonophoresis occurs because ultrasound waves stimulate micro-vibrations within the skin epidermis and increase the overall kinetic energy of molecules When sound is emitted at a particular frequency, the sound waves disrupt the lipid bilayers The higher the frequency, the more dispersed the transmission
The skin
Protective layer with large no. of dead cells, hence acts as barrier to penetration. Penetration varies with humidity, pigmentation, age, chemical status Of all layers Stratum Corneum (SC) offers maximum resistance. SC consists of keratinocytes and lipid bilayer Permeability can be increased by Chemicals, Electrical Fields or Ultrasound which disrupt lipid bilayer of SC and increase permeability.
3. Generation of ultrasound
Ultrasound is a sound wave possessing frequencies above 20 kHz . These waves are characterized by two main parameters, frequency and amplitude The waves used for sonophoresis which reduce the resistance offered by SC lie in the frequency range of 20 KHz to 20 MHz Ultrasound is generated with the help of a device called sonicator which is a AC electric signal generator. It produces a AC electric signal which is applied across a piezoelectric crystal i.e. transducer.
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Ultrasound is applied by bringing the transducer in contact with the skin. For sonophoretic delivery, the desired drug is dissolved in a solvent and applied to the skin. The coupling medium can be the same as the solvent used to dissolve the drug or it can be a commercial ultrasound coupling e.g. gel. It Helps to match impedence of tissue with the impedence of the transducer, so that the Ultrasound gets properly into the tissue.
Therapeutic Frequency Ultrasound (1-3 MHz) Low Frequency Ultrasound (Below 1MHz) High Frequency Ultrasound (Above 3MHz)
Ultrasound can be applied in a continuous or pulse mode. The pulse mode is frequently used because it reduces severity of side effects such as thermal effects. It was also found that urea permeability of cuprophane membrane increased from 6 to 56% as pulse length increased from 100 to 400 ms.
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(2) Cavitation effect may important when,
Low-frequency ultrasound is used Grassy fluids are exposed Small gas filled space are exposed The tissue temperature is higher than normal
surrounding The fluids in the biological medium is free to more Continuous wave application is used
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5. Mechanism of sonophoresis
(1) Cavitation
Cavitation occurs due to the nucleation of small gaseous
cavities during the negative pressure cycles of ultrasound This cavitation leads to the disordering of the lipid bilayers and formation of aqueous channels in the skin through which drugs can permeate
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The minimum ultrasound intensity required for the onset
interfaces may, in turn cause oscillations in the lipid bilayers, thereby causing structural disorder of the SC lipids
observed transdermal transport enhancement. these bubbles cause skin erosion, due to generation of shock waves, thereby enhancing transdermal transport
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(2) Convective transport
Fluid velocities generated in this way may affect
transdermal transport by inducing convective transport of the permeant across the skin. especially through hair follicles and sweat ducts
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(3) Mechanical stress
Ultrasound is a longitudinal pressure wave inducing pressure variations in the skin, which, in turn, induce density variation Due to density variations, such as generation of cyclic stresses because of density changes that ultimately lead to fatigue of the medium Lipid bilayers, being self-assembled structures, can easily be disordered by these stresses, which result in an increase in the bilayers permeability
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e.g. Application of SLS alone for 90 min induced about 3fold increase in mannitol permeability, while application of ultrasound alone for 90 min induced about 8-fold enhancement. However, when combined, application of ultrasound from 1% SLS solution induced about 200-fold increase in skin permeability to mannitol
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(2) Iontophoresis
Electrophoresis Lipid Bilayer Disordering Electroosmosis
e.g. The enhancement of heparin flux due to ultrasound +
iontophoresis treatment was about 56-fold. This enhancement was higher than the sum of those obtained during ultrasound alone (3-fold) and iontophoresis alone (15-fold). Thus, the effect of ultrasound and iontophoresis on transdermal heparin transport was truly synergistic.
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7.Safety
The World Federation for Ultrasound in Medicine and Biology (WFUMB) has issued several publications related to safety of ultrasound bioeffects, addressing specifically thermal bioeffects and non-thermal bioeffects ultrasound affecting the structure of the skin: is it a reversible or irreversible change? What is the role of the free radicals that are generated during the cavitation process within the skin?
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8. Applications
1) Sonophoresis is used in the treatment of damaged skin. 2) Hormone Delivery. 3) In surgery it helps in dissection, connection, built-up and treatment of biological tissue. 4) Low-Frequency Ultrasonic Gene Delivery. 5) Sonophoresis is also very useful in drug enhancement in granulomas and tumors. Most cancer therapy drugs act intracellularly. 6) Ultrasound is used for Calcific Tendinitis of the Shoulder. 7) The dolphin therapy and sonophoretic model. 8) Ultrasound Helps in Treating Tennis Elbow and Tendon Problem.
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9. Advantages
1) Avoids vagaries associated with gastrointestinal absorption due to pH, enzymatic activity, drug-food interactions etc. 2) Substitute oral administration when the route is unsuitable as in case of vomiting, diarrhea. 3) Avoids hepatic first pass effect. 4) Avoids the risks and inconveniences of parenteral therapy. 5) Reduces daily dosing, thus, improving patient compliance. 6) Extends the activity of drugs having short plasma half-life through the reservoir of drug present in the therapeutic delivery system and its controlled release characteristics. 7) Rapid termination of drug effect by removal of drug application from the surface of the skin. 8) Rapid identification of the medication in emergencies. (e.g.. Non-responsive, unconscious, or comatose patient.)
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9) Elimination of the hazards and difficulties of I.V. infusions or I.M. injections. 10) Enhance therapeutic efficacy, reduced side effects due to optimization of the blood concentration-time profile and elimination of pulse entry of drugs into the systemic circulation. 11) Provide predictable activity over extended duration of time and ability to approximate zero-order kinetics. 12) Improved control of the concentrations of drug with small therapeutic indices. 13) Minimize inter and intrapatient variation. 14) Suitability for self-administration.
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10. Limitations
1) Only limited number of potent drugs can be absorbed in therapeutic dose. 2) Many systemically effective therapeutic drugs produce skin irritation. 3) The drug must have some desirable physicochemical properties for penetration through stratum corneum. 4) If the drug dosage required for therapeutic value is more than 10mg/day, the transdermal delivery will be very difficult.
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to enhanced the delivery of steroidal anti-inflammatory drugs (e.g. hydrocortisone). (a) Fellinger & Schmid (1954) showed that ultrasound could carry hydrocortisone across a vascular membrane for the effective treatment of polyarthritis (b) Newman et al. (1992) suggested that hydrocortisone sonophoresis is useful in the treatment of numerous musculo-skeletal injuries.
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(2) Sonophoresis with Salicylates
In combination with ultrasound it is thought that
Salicylate could be moved into deeper, subdermal tissues to help to reduce pain. (a) Ciccone et al. (1991) reported on a study to evaluate ultrasound as an enhancer of topically applied Salicylates
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(3) Sonophoresis with Anesthetics
The effectiveness of sonophoresis has been explored
extensively for delivery of local anesthetics. (a) McElnay (1985) and associates described a sonophoresis study using lignocain (b) Moll (1979) studied the enhanced effects of topically applied Lidocaine (140.7 mg) and Decadron (3.75 mg). She obtained that 88% of the patients receiving sonophoresis with Decadron and Lidocaine obtained relief from their trigger point pain.
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(4) Sonophoresis with other Drugs
(a) Benson and colleagues (1987, 1989) studied ultrasound as an enhancer of benzydamine hydrochloride (3%) a nonsteroidal anti-inflammatory drug. (b) Levy et al. (1989) studied the sonophoresis of Dmannitol, a diuretic. (c) Romanenko (1992) used ultrasound with topically applied Amphotericin B.
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Sr Sonophoresis no 1 Sonophoresis is the enhancement of migration of drug molecules through the skin by ultrasonic energy 2 Sonophoresis uses acoustic energy (ultrasound) to drive molecules into tissues 3 Proper choice of ultrasound parameters including ultrasound energy dose, frequency, intensity, pulse length, and distance of transducer from the skin is critical for efficient sonophoresis. 4 Sonophoresis usually employs a ultrasound between 20 KHz to 20 MHz
Iontophoresis Iontophoresis is movement of ions of soluble salts across a membrane under an externally applied potential difference Iontophoresis uses electiral current to transport ions into tissues Proper choice of electricity parameters including Current density, Current profile, Duration of treatment, Electrode material, Polarity of electrodes, is critical for efficient Iontophoresis Iontophoresis usually employs a direct current between 0.5 mA to 5.0 mA
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In sonophoresis drugs mixing with a coupling agent like gel, cream, ointment The main mechanism for transport of drug is Cavitation Drug should be in aqueous or non aqueous and ionized or non ionized form Enhanced partitioning, Lipid bilayer disordering, Keratin denaturation etc. gives the synergetic effect of sonophoresis Ultrasound can be applied in a continuous or pulse mode
In Iontophoresis drug is mix with solvent The main mechanism for transport of drug is Electroporation Drug must be in aqueous and must be in ionized form Electrophoresis, Lipid bilayer disordering, Electroosmosis etc. gives the synergetic effect of Iontophoresis Electrical current can be applied only in continuous mode
10 Sonophoresis mostly used for Iontophoresis mostly used for delivery of corticosteroids, local hyperhydrosis diagnosis of cystic anesthetics and salicylates fibrosis, metallic and non-metallic ions
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12. Conclusion
Proper choice of ultrasound parameters including
ultrasound energy dose, frequency, intensity, pulse length, and distance of transducer from the skin is critical for efficient sonophoresis. Various studies have indicated that application of ultrasound under conditions used for sonophoresis does not cause any permanent damage to the skin Ultrasound also works synergistically with several other enhancers including chemicals and iontophoresis.
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13. References
N.K.Jain, Sonophoresis: Biophysical of Transdermal Drug Delivery, Controlled and Novel Drug Delivery, 1st edition, 1997, page. 208-235 James Swarbrick, Transdermal Delivery: Sonophoresis, Encyclopedia of pharmaceutical technology, 3rd edition, Volume-6, 2007, page no. 3828-3842 Mr. Ashish Pahade, Dr. Mrs. V.M.Jadhav, Dr. Mr. V.J.Kadam, Sonophoresis: an overview, International Journal of Pharmaceutical Science, 2010, Volume 3, Issue 2, page. 24-32 V.M. Meidan a, A.D. Walmsley b, W.J. Irwin, Phonophoresis is it a reality? International Journal of Pharmaceutics 118 :1995 page.129-149 http://www.dolphintherapy.ru/en/sonoforez.shtml
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