Next Article in Journal
Targeted Nanomedicine to Treat Bone Metastasis
Next Article in Special Issue
Nanoemulsion as a Platform for Iontophoretic Delivery of Lipophilic Drugs in Skin Tumors
Previous Article in Journal
Advanced Pharmaceutical Applications of Hot-Melt Extrusion Coupled with Fused Deposition Modelling (FDM) 3D Printing for Personalised Drug Delivery
Previous Article in Special Issue
Iontophoretic Transdermal Delivery of Human Growth Hormone (hGH) and the Combination Effect of a New Type Microneedle, Tappy Tok Tok®
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:

Selected Medicines Used in Iontophoresis

Department of Medical Microbiology, Poznań University of Medical Sciences, Wieniawskiego 3, 61-712 Poznań, Poland
Pharmaceutics 2018, 10(4), 204;
Received: 19 September 2018 / Revised: 17 October 2018 / Accepted: 24 October 2018 / Published: 25 October 2018


Iontophoresis is a non-invasive method of systemic and local drug delivery using an electric field. Iontophoresis enables diffusion of the selected drug via skin, mucosa, enamel, dentin, and other tissues. The amount of delivered therapeutic molecules is about 10–2000 times greater than conventional forms of delivery. Among other fields, this method is used in dentistry, ophthalmology, otorhinolaryngology, and dermatology. According to related literature, the most important drugs studied or administered by iontophoresis are: Local anesthetics, opioids, steroids, non-steroidal anti-inflammatory drugs, antibacterial drugs, antifungal drugs, antiviral drugs, anticancer drugs, fluorides, and vitamins. The present review covers current available data regarding the selected medicines used in iontophoresis. Furthermore, indications and conditions of iontophoresis application are reviewed.

1. Introduction

Iontophoresis is a type of electrotherapy, during which a drug is introduced deep into the tissues as a means of systemic and local drug application [1]. It is based on the principle that in a given electric field, positively charged drug ions (cations) are repelled by a positive electrode (anode) and are directed to the cathode (Figure 1). In turn, negative ions (anions, e.g., ketoprofen) being repelled by the negative electrode (cathode), follow the anode. The optimal molecules for use with iontophoresis are small and hydrophilic [2]. The penetration of the drug substance takes place through the skin, sweat glands and sebaceous glands, which enables diffusion to deeper layers of tissues, even 48 h after the procedure [3]. Iontophoresis allows delivery of about 10–2000 times more polar hydrophilic therapeutic molecules than typical application of a drug substance to the skin surface [4].
There are various factors affecting iontophoresis. Direct current is most commonly used, however in study of Zhu et al. alternating current (AC) iontophoresis showed better results than conventional constant current DC iontophoresis [5]. The drug used should be water-soluble, of low-dosage and susceptible to ionization. Smaller particles are more mobile. Increasing drug concentration results in greater drug delivery, but only to some extent. If buffer ions are present, they compete with the drug, reducing its delivery. The effect of iontophoresis also depends on the tissue on which the electrodes are applied (e.g., thickness, permeability, the presence of pores). In the skin, sweat glands are the most significant way the charges are carried [6].
The iontophoresis process uses two types of voltage supply—direct current and alternating current. The most commonly used method is direct current iontophoresis [8]. Among other fields, this method is used in dentistry, ophthalmology, otorhinolaryngology, and dermatology for the administration of local anesthetics, non-steroidal anti-inflammatory drugs, antibiotics, anticancer drugs, hormones, as well as other substances [8,9,10].
Some of the outstanding features of iontophoresis are its safety, high transdermal efficiency, and simplicity of application [11]. In contrast to other techniques, iontophoresis acts more on the molecules of medicine and less so on the skin [12]. However, direct current iontophoresis can cause side effects, such as burns, redness and skin irritation [8,13]. One significant problem of this method is that only potent molecules can be delivered [14].
Contraindications associated with the action of the galvanic current, as well as allergic drug reactions are:
  • Superficial and deep sensory disorders;
  • Should not be used in pregnancy;
  • Should not be used during lactation;
  • Hypersensitivity to the active substance [4,15,16].
The present review summarizes information about iontophoresis of the selected medicines from the following groups: Local anesthetics, opioids, steroids, non-steroidal anti-inflammatory drugs, antibacterial drugs, antifungal drugs, antiviral drugs, anticancer drugs, fluorides, and vitamins (Table 1).

2. Local Anesthetics

Local anesthetics are drugs that cause a reversible absence of pain sensation [79]. Smitayothin et al. presented the anesthetized effect of iontophoresis of lignocaine with epinephrine on dentine for cavity preparation. The cavities of 56 molar teeth were filled with 20% lidocaine with 0.1% epinephrine. Iontophoretic anodal at 200 mA current was applied for 2 min. If the dentine was not anaesthetized, the treatment was repeated up to six times. Time of iontophoresis duration required to anaesthetize the dentine varied from: Two min for 7 teeth, 4 min for 17 teeth, 6 min for 14 teeth, 8 min for 4 teeth and up to 10 min for seven teeth. Not all studied teeth were anaesthetized. In 7 of the treated teeth, no effect was observed after 14 min of iontophoresis. Ultimately, 87.5% of the studied molars with caries were anesthetized by iontophoretic delivery of lignocaine with epinephrine [56]. Using lignocaine plus epinephrine solution iontophoresis on teeth caries immediately inhibits the pain and continues for at least 40 min [57]. In comparison, a locally applied solution of 50% lignocaine without iontophoresis produces anesthesia for a maximum of 10 min and after a latent period for up to 30 min [80].
The anesthetic effect of lidocaine is significantly increased after adding epinephrine and is dose-related. A concentration of epinephrine higher than 1:160,000 enhances and prolongs the anesthetic effect during the iontophoresis of lidocaine [48]. It was found that 2% lidocaine with epinephrine can be delivered up to 5 mm below the surface of the skin [55].
Inoue et al. presented that lidocaine is delivered in iontophoresis more rapidly with direct current than with alternating current. Moreover, ions are transported faster when voltage is switched from direct current to alternating current. They found that iontophoresis in combination with direct current and alternating current enabled highly efficient drug delivery [8].
It was also shown that lidocaine hydrochloride can pass through enamel/dentine by using alternating current iontophoresis [51]. This method may avoid the numbness observed when the anesthetic is administered with a syringe [81]. The permeability of enamel/dentine may function as a novel drug delivery system. Using this system of iontophoresis, antibiotics and nonsteroidal anti-inflammatory drugs (NSAIDs) can be administered in order to alleviate inflammation and pulpal pain or dentine hypersensitivity following bleaching or acid etching of enamel [51,82]. Saliba et al. demonstrated that high amplitude/short duration or low amplitude/long duration of lidocaine iontophoresis does not affect the anesthetic level when the same dosage is applied [83].

3. Opioids

The fentanyl HCl iontophoretic transdermal system (fentanyl ITS) has been approved in the US and Europe. This system ensures patient-controlled analgesia in acute and moderate-to-severe postoperative pain [84]. Fentanyl ITS is considered an equivalent method of pain control comparative to standard intravenous delivery of morphine [37]. The described system also decreases staff assistance time required for helping patients and accelerates the anesthetic effect [85].

4. Steroids

Iontophoresis is used as a non-invasive method for administration of dexamethasone into the eye for the treatment of uveitis and other inflammatory eye conditions. It was demonstrated that iontophoresis enhances penetration and distribution of a combination of dexamethasone and dendrimers into the cornea [33]. A study with patients suffering from dry eye revealed that receiving dexamethasone phosphate (EGP-437) solution via ocular iontophoresis led to reducing unwanted signs and symptoms [86]. Iontophoretic application of dexamethasone phosphate (EGP-437) into ocular tissues can also be used for therapy of anterior uveitis [87] and ocular inflammation post cataract surgery [88].
Some studies have also considered the use of dexamethasone in iontophoresis for treating disorders of temporomandibular joints. Dexamethasone/dexamethasone phosphate can be delivered to depths of up to 12 mm [89]. For disorders of temporomandibular joints, dexamethasone iontophoresis improves function, including motion and affects decreasing pain [32,90].

5. Non-Steroidal Anti-Inflammatory Drugs

Non-steroidal anti-inflammatory drugs (NSAIDs) have anti-inflammatory, analgesic and antipyretic properties. Data from literature indicate that the use of NSAIDs in percutaneous iontophoresis of temporomandibular joints relieves pain in rheumatoid arthritis, joint injuries and for patients with masticatory dysfunction [91,92]. The application is also used in post-traumatic conditions (e.g., dislocation of the temporomandibular joints), overload conditions (e.g., in the course of bruxism), chronic inflammatory and degenerative-inflammatory processes, neuralgias, lockjaw, tooth hyperalgesia and postoperative pain [93]. NSAIDs used in iontophoresis are applied omitting oral administration and thus save the gastrointestinal tract, especially for patients with diseases and dysfunctions of the digestive system [3].
Ketoprofen given percutaneously penetrates well into temporomandibular joints. It was found that the higher the activity of the synovium inflammatory process, the better the penetration of the drug into the joint cavity [94]. The cationic ester prodrug of ketoprofen highly reduced plasma protein binding. Anodal iontophoresis of the cationic ester prodrug of ketoprofen is characterized by enhanced delivery efficiency and increased drug retention in the skin and has potential in topical therapy of musculoskeletal diseases [47].
Other NSAIDs used in iontophoresis are aspirin, ibuprofen, and indomethacin. The studied NSAIDs administered by iontophoresis showed a higher anti-inflammatory effect in rats than drugs administered without iontophoresis. Iontophoresis significantly improved penetration of aspirin, ibuprofen, and indomethacin into the hypodermis, dermis and epidermis [11]. In the case of celecoxib using iontophoresis enhanced transdermal flux through rat skin resulted in almost twice as much drug transport in comparison to passive diffusion. Iontophoretic application of celecoxib can be used in the treatment of osteoarthritis, acute pain, joint inflammation and joint injuries [26].
In studies on humans, iontophoretic delivery of diclofenac demonstrated measured plasma concentrations of this drug in 75% of participants. However, in the group without iontophoresis only in 25% of the subjects was diclofenac detected in their plasma. The authors suggested that iontophoresis failed to achieve more effective local concentrations of diclofenac [35]. Arunkumar et al. used terpenes (geraniol, l-menthol and thymol) as iontophoretic efficiency enhancers. They presented the effect of terpenes on iontophoresis of diclofenac. Geraniol and l-menthol enhanced the iontophoretic flux, decreased the percent of inflammation, and enabled safer iontophoresis of diclofenac [95].
Presence of dental caries may inhibit drug delivery from dentine to the pulp. Puapichartdumrong et al. investigated the role of iontophoresis in drug delivery through human intact dentine and dentine affected with caries. The diffusion of metronidazole, sodium salicylate, and naproxen sodium was significantly less through dentine with caries than those without a cavity. Simultaneously, iontophoresis enhanced the delivery of drugs [58].

6. Antibacterial Drugs

Iontophoresis can be used as a method of disinfection against biofilm in teeth root canals. Gergova et al. showed that potassium iodide iontophoresis was most effective against biofilm caused by Gram-positive cocci. A very good bactericidal effect was also obtained by iontophoresis with Cupral (Cu). The authors emphasize that iontophoretic disinfection is a non-invasive and low-cost method [29].
Some studies on animals have shown the influence of antibiotics when used in ocular iontophoresis. Choi and Lee presented that transscleral and transcorneal iontophoresis (0.5 mA for 5 min) is suitable for application of vancomycin into the aqueous and vitreous humor and the cornea of rabbit eyes [77]. Research, has shown that transscleral transport of vancomycin does not increase linearly with either an increase of current density or antibiotic concentration [78]. Rabbits were also used to study transcorneal iontophoresis for delivery of ciprofloxacin. The authors described this method as being useful for ciprofloxacin delivery into the aqueous humor for the treatment of intraocular infections [28]. Iontophoresis of hydrogel containing gentamicin can be used for eye infections. Rabbits were used as subjects to describe the potential clinical effect of gentamicin-loaded hydrogels in treating corneal infections caused by Pseudomonas aeruginosa [44]. Iontophoresis increased also concentration of amikacin in rabbit eye and skin [22,23].
Iontophoresis is a promising method for fast application of amoxicillin and cefuroxime into the skin. In the case of amoxicillin, therapeutic concentrations in the skin were detected immediately after the application and remained for at least two h. For cefuroxime, therapeutic skin concentrations were obtained only at higher current densities [25]. In studies of Puapichartdumrong et al. diffusion of metronidazole, drug used against anaerobic bacteria, was significantly influenced by iontophoresis [58].
Silver also possesses antibacterial activity. Iontophoresis with a silver-polymer-based surface system caused a high antibacterial effect against Gram-negative bacteria (Escherichia coli, and Pseudomonas aeruginosa) and low effect against Gram-positive bacteria (Staphylococcus aureus and Enterococcus faecalis) [64].
Application of anodal iontophoresis using silk fibroin and neurotensin caused the release of high neurotensin concentrations in a short period. This type iontophoresis had an additional bacteriostatic effect against Gram-positive Staphylococcus aureus and S. epidermidis, without causing toxicity to fibroblasts [63]. Whereas, anodal iontophoresis at pH 4.0 increased transport and accumulation of amikacin used topically for the treatment of ocular infections [23].

7. Antifungal Drugs

Grossman and Lee described that ketoconazole concentrations in aqueous humor and cornea of the rabbit eye were significantly higher after transscleral and transcorneal iontophoresis [46]. Sachdeva et al. applied terbinafine hydrochloride to the skin using anodal iontophoresis. It was observed that iontophoresis delivered higher drug levels to the deeper skin as compared to control subjects. The drug was detectable in the skin for at least two days following iontophoretic treatment [76]. Terbinafine provides fungicidal activity against dermatophytes (Trichophyton, Microsporum, and Epidermophyton), molds and certain dimorphic fungi. When used against fungi of the genera Candida and Malassezia it either acts as fungicidal or fungistatic, depending on the species [96].

8. Antiviral Drugs

Siddoju et al. described the use of iontophoresis for improved topical delivery of acyclovir. Acyclovir is used to treat Herpes simplex and Varicella-zoster virus infections. Iontophoresis was performed for 10 min on rats using a 5% acyclovir gel. The method resulted in high acyclovir levels in skin layers for up to 2–3 days [20]. Transscleral iontophoresis of acyclovir prodrugs (ACV-X, X = Arg, Gly and Trp) achieves a higher concentration and faster delivery rate of acyclovir. Iontophoresis of ACV-Gly for 5 min leads to a higher level of acyclovir than IC50 against HSV-1. This method is useful for the treatment of herpetic infections in the anterior and posterior segments of the eye [21].

9. Anti-Cancer Drugs

Local iontophoretic chemotherapy treatment at various stages of cancer can be an addition to surgery, radiation, and systemically administered chemotherapy. Local treatment leads to the reduction of drug side effects and is suggested for drugs which are too toxic when delivered systemically [97,98]. The iontophoretic application of anticancer agents can act transdermal, transpapillary, intravesical, transscleral, and peri-pancreatic [10].
Cisplatin and 5-fluorouracil are drugs used in the treatment of skin basal cell and squamous cell carcinoma. Iontophoretic application of 5-fluorouracil led to no clinical or histologic evidence of residual squamous cell carcinoma three months after the last treatment in 25 of 26 patients [99]. The effect of local administration of 5-fluorouracil combined with immunoliposomes using iontophoresis against squamous cell carcinoma was also described [39]. The cisplatin iontophoresis was used successfully in a patient with basal cell carcinoma. The effectiveness of the treatment was confirmed by biopsies, which revealed no evidence of basal cell carcinoma [100].
Chemotherapeutic agents to treat head and neck cancers can be delivered using buccal iontophoresis. Cathodal iontophoresis of 5-fluorouracil and leucovorin increased the mucosal deposition of both drugs. An 8-fold enhancement of deposition for 5-fluorouracil and a 3-fold increase for leucovorin was observed [38].
Iontophoretic cancer treatment was used to apply nanocomplex STAT3 siRNA (a small interference RNA) with success in preclinical studies [101]. STAT3 (signal transducer and activator of transcription 3) is an oncogenic transcription factor which is activated in multiple cancer types, including skin cancer [102]. Topical iontophoresis of curcumin with STAT3 siRNA complex enhanced skin penetration of the nanocomplex and can be developed for skin cancer treatment [30]. Iontophoretic anodal application of STAT3 siRNA complex and imatinib mesylate had a suppressive effect on melanoma cancer [75].
Another possibility of iontophoretic cancer treatment is for administering anti-cancer vaccines. Toyoda et al. studied nanogels containing gp-100 peptide KVPRNQDWL as a potential component of anti-cancer vaccines against melanoma in mice. The iontophoresis improved transport of the nanogels into the skin, as well as accumulation of Langerhans cells. Finally, melanoma growth in mice was significantly suppressed by this method [45].
Iontophoresis for anticancer therapy is also used in connection with other methods. One example is a combination of direct-current pulsed iontophoresis along with photodynamic therapy. These two combined methods can be used for application of 5-aminolevulinic acid for skin cancer. Patients with actinic keratosis who were treated with iontophoresis and photodynamic treatment had complete recovery [24].

10. Fluorides

Fluoride iontophoresis can be used for reduction of dentinal hypersensitivity and remineralization of enamel. Patients affected by dentinal hypersensitivity have symptoms reacting to hot, cold, chilled, acidic or sweet liquids and food. Fluoride ions react with calcium ions forming acid-resistant calcium fluoride which blocks dentinal tubules [68]. It was demonstrated that iontophoresis with 2% sodium fluoride (NaF) solution is more effective in reduction of hypersensitivity than local application of 2% NaF or HEMA-G iontophoresis. Measurements at 3-month intervals of administering 2% NaF iontophoresis indicated the best long-lasting effect [70]. A similar effect was observed Singal et al. The Authors compared reduction of dentinal hypersensitivity after using 2% NaF iontophoresis and an aqueous solution of HEMA-G. NaF iontophoresis had a more significant effect in the 1- and 3-month intervals than HEMA-G [67].
Using in vitro studies, fluoride iontophoresis was compared with the conventional application of fluoride. Bovine enamel samples were covered with 3 mL of fluoride (1.23% acidulated phosphate fluoride (APF) gel and 2% sodium fluoride (NaF) solution) for 4 min each 5 days. The iontophoresis study group was electrically charged for 4 min each five days. In this experiment, fluoride iontophoresis was not significantly better than conventional fluoride application regarding the remineralization effect [18].
In other studies, also based on bovine enamel, the most effective treatment was acidulated phosphate fluoride gel application, followed by 5% NaF varnish application and 2% NaF iontophoresis. In the NaF iontophoresis group the fluoride uptake was higher, and cavity depth was smaller, in comparison to the control group. However, NaF iontophoresis had a significantly lower effect on the remineralization than that of acidulated phosphate fluoride gel [69].

11. Vitamins

Iontophoresis with dextran-free 0.1% riboflavin-5-phosphate (Vitamin B2) solution was used in a randomized study of patients with progressive keratoconus. Iontophoresis was delivered along with irradiating the cornea with a 10 mW/cm2 ultraviolet A for 9 min. One year following iontophoresis significant visual and refractive improvements were reported. Simultaneously, no complications occurred in this patient group [62]. Other studies have shown inhibition of keratoconus progression within 24 months, resulting in a significant improvement in visual and topographic parameters. Riboflavin (0.1%) was used in iontophoresis-assisted corneal crosslinking [61]. Application of riboflavin in corneal stroma by iontophoresis for halting keratoconus progression was also suggested by Mencucci et al. [59].
An animal model was tested using riboflavin/ultraviolet-A iontophoresis-assisted cross-linking procedure for the treatment of myopia. Riboflavin (0.1%) was used as a photosensitizer and the duration of iontophoresis was 10 min. This combination of methods was deemed effective and safe to control the pathologic process of myopia [60].

12. Summary

To summarize, iontophoresis is a valuable, non-invasive method, which can be used for topical treatment of pain, inflammation, infections, and cancers. Some medicines, e.g., lignocaine or sodium fluoride are already administered by iontophoresis to patients. Other medicines are under in vitro investigations or undergoing animal studies and have shown potential for applying them for delivery of different medicines. Further research should be performed especially on the effectiveness of delivering non-ionic drugs using this method.

Conflicts of Interest

The author declares no conflict of interest.


  1. Ebisawa, T.; Nakajima, A.; Haida, H.; Wakita, R.; Ando, S.; Yoshioka, T.; Ikoma, T.; Tanaka, J.; Fukayama, H. Evaluation of calcium alginate gel as electrode material for alternating current iontophoresis of lidocaine using excised rat skin. J. Med. Dent. Sci. 2014, 61, 41–48. [Google Scholar] [CrossRef] [PubMed]
  2. Dhote, V.; Bhatnagar, P.; Mishra, P.K.; Mahajan, S.C.; Mishra, D.K. Iontophoresis: A potential emergence of a transdermal drug delivery system. Sci. Pharm. 2012, 80, 1–28. [Google Scholar] [CrossRef] [PubMed]
  3. Kowalska, M. Zastosowanie ketoprofenu w jonoforezie. Ketoprofen in iontophoresis. Pediatr. Med. Rodz. 2011, 7, 124–128. [Google Scholar]
  4. Straburzyńska-Lupa, A.; Straburzyński, G. Fizjoterapia; PZWL: Warszawa, Poland, 2004; pp. 481–492. [Google Scholar]
  5. Zhu, H.; Li, S.K.; Peck, K.D.; Miller, D.J.; Higuchi, W.I. Improvement on conventional constant current DC iontophoresis: Study using constant conductance AC iontophoresis. J. Control. Release 2002, 82, 249–261. [Google Scholar] [CrossRef]
  6. Rai, R.; Srinivas, C.R. Iontophoresis in dermatology. Indian J. Dermatol. Venereol. Leprol. 2005, 71, 236–241. [Google Scholar] [CrossRef] [PubMed]
  7. Wanasathop, A.; Li, S.K. Iontophoretic drug delivery in the oral cavity. Pharmaceutics 2018, 10, 121. [Google Scholar] [CrossRef] [PubMed]
  8. Inoue, T.; Sugiyama, T.; Ikoma, T.; Shimazu, H.; Wakita, R.; Fukayama, H. Drug delivery and transmission of lidocaine using iontophoresis in combination with direct and alternating currents. J. Med. Dent. Sci. 2016, 63, 71–77. [Google Scholar] [CrossRef] [PubMed]
  9. Huang, D.; Chen, Y.S.; Rupenthal, I.D. Overcoming ocular drug delivery barriers through the use of physical forces. Adv. Drug Deliv. Rev. 2018, 126, 96–112. [Google Scholar] [CrossRef] [PubMed]
  10. Byrne, J.D.; Yeh, J.J.; DeSimone, J.M. Use of iontophoresis for the treatment of cancer. J. Control. Release 2018, 284, 144–151. [Google Scholar] [CrossRef] [PubMed]
  11. Zuo, J.; Du, L.; Li, M.; Liu, B.; Zhu, W.; Jin, Y. Transdermal enhancement effect and mechanism of iontophoresis for non-steroidal anti-inflammatory drugs. Int. J. Pharm. 2014, 466, 76–82. [Google Scholar] [CrossRef] [PubMed]
  12. Ita, K. Transdermal delivery of vaccines–Recent progress and critical issues. Biomed. Pharmacother. 2016, 83, 1080–1088. [Google Scholar] [CrossRef] [PubMed]
  13. Ledger, P.W. Skin biological issues in electrically enhanced transdermal delivery. Adv. Drug Deliv. Rev. 1992, 9, 289–307. [Google Scholar] [CrossRef]
  14. Ita, K. Transdermal iontophoretic drug delivery: Advances and challenges. J. Drug Target. 2016, 24, 386–391. [Google Scholar] [CrossRef] [PubMed]
  15. Spodaryk, K.; Bromboszcz, J. Fizykoterapia—Potrzeba badań naukowych. Rehabil. Med. 2004, 8, 8–14. [Google Scholar]
  16. Samborski, W.; Ponikowska, I. Choroby reumatyczne—Standardy leczenia w medycynie uzdrowiskowej. Balneol. Pol. 2005, 1–2, 14–23. [Google Scholar]
  17. Kralinger, M.T.; Voigt, M.; Kieselbach, G.; Hamasaki, D.; Hayden, B.; Parel, J.M. Ocular delivery of acetylsalicylic acid by repetitive coulomb-controlled iontophoresis. Ophthalmic Res. 2002, 35, 102–110. [Google Scholar] [CrossRef] [PubMed]
  18. Kim, H.E.; Kwon, H.K.; Kim, B.I. Application of fluoride iontophoresis to improve remineralization. J. Oral Rehabil. 2009, 36, 770–775. [Google Scholar] [CrossRef] [PubMed]
  19. Girenes, G.; Ulusu, T. An in vitro evaluation of the efficacy of a novel iontophoresis fluoride tray on remineralization. J. Clin. Exp. Dent. 2014, 6, e327–e334. [Google Scholar] [CrossRef] [PubMed]
  20. Siddoju, S.; Sachdeva, V.; Friden, P.M.; Yu, Y.Y.; Banga, A.K. Acyclovir skin depot characterization following in vivo iontophoretic delivery. Skin Res. Technol. 2011, 17, 234–244. [Google Scholar] [CrossRef] [PubMed]
  21. Chen, Y.; Kalia, Y.N. Short-duration ocular iontophoresis of ionizable aciclovir prodrugs: A new approach to treat herpes simplex infections in the anterior and posterior segments of the eye. Int. J. Pharm. 2018, 536, 292–300. [Google Scholar] [CrossRef] [PubMed]
  22. Vollmer, D.L.; Szlek, M.A.; Kolb, K.; Lloyd, L.B.; Parkinson, T.M. In vivo transscleral iontophoresis of amikacin to rabbit eyes. J. Ocul. Pharmacol. Ther. 2002, 18, 549–558. [Google Scholar] [CrossRef] [PubMed]
  23. Nicoli, S.; Santi, P. Transdermal delivery of aminoglycosides: Amikacin transport and iontophoretic non-invasive monitoring. J. Control. Release 2006, 111, 89–94. [Google Scholar] [CrossRef] [PubMed]
  24. Mizutani, K.; Watanabe, D.; Akita, Y.; Akimoto, M.; Tamada, Y.; Matsumoto, Y. Photodynamic therapy using direct-current pulsed iontophoresis for 5-aminolevulinic acid application. Photodermatol. Photoimmunol. Photomed. 2009, 25, 280–282. [Google Scholar] [CrossRef] [PubMed]
  25. Mannem, V.; Nanjarapalle, C.; Stagni, G. Iontophoresis of amoxicillin and cefuroxime: Rapid therapeutic concentrations in skin. Drug Dev. Ind. Pharm. 2014, 40, 325–329. [Google Scholar] [CrossRef] [PubMed]
  26. Tavakoli, N.; Minaiyan, M.; Heshmatipour, M.; Musavinasab, R. Transdermal iontophoretic delivery of celecoxib from gel formulation. Res. Pharm. Sci. 2015, 10, 419–428. [Google Scholar] [PubMed]
  27. Hobden, J.A.; Reidy, J.J.; O’Callaghan, R.J.; Insler, M.S.; Hill, J.M. Ciprofloxacin iontophoresis for aminoglycoside-resistant pseudomonal keratitis. Investig. Ophthalmol. Vis. Sci. 1990, 31, 1940–1944. [Google Scholar]
  28. Vaka, S.R.; Sammeta, S.M.; Day, L.B.; Murthy, S.N. Transcorneal iontophoresis for delivery of ciprofloxacin hydrochloride. Curr. Eye Res. 2008, 33, 661–667. [Google Scholar] [CrossRef] [PubMed]
  29. Gergova, R.T.; Gueorgieva, T.; Dencheva-Garova, M.S.; Krasteva-Panova, A.Z.; Kalchinov, V.; Mitov, I.; Kamenoff, J. Antimicrobial activity of different disinfection methods against biofilms in root canals. J. Investig. Clin. Dent. 2016, 7, 254–262. [Google Scholar] [CrossRef] [PubMed]
  30. Jose, A.; Labala, S.; Venuganti, V.V. Co-delivery of curcumin and STAT3 siRNA using deformable cationic liposomes to treat skin cancer. J. Drug Target. 2017, 25, 330–341. [Google Scholar] [CrossRef] [PubMed]
  31. Smutok, M.A.; Mayo, M.F.; Gabaree, C.L.; Ferslew, K.E.; Panus, P.C. Failure to detect dexamethasone phosphate in the local venous blood postcathodic lontophoresis in humans. J. Orthop. Sports Phys. Ther. 2002, 32, 461–468. [Google Scholar] [CrossRef] [PubMed]
  32. Mina, R.; Melson, P.; Powell, S.; Rao, M.; Hinze, C.; Passo, M.; Graham, T.B.; Brunner, H.I. Effectiveness of dexamethasone iontophoresis for temporomandibular joint involvement in juvenile idiopathic arthritis. Arthritis Care Res. 2011, 63, 1511–1516. [Google Scholar] [CrossRef] [PubMed][Green Version]
  33. Souza, J.G.; Dias, K.; Silva, S.A.; de Rezende, L.C.; Rocha, E.M.; Emery, F.S.; Lopez, R.F. Transcorneal iontophoresis of dendrimers: PAMAM corneal penetration and dexamethasone delivery. J. Control. Release 2015, 200, 115–124. [Google Scholar] [CrossRef] [PubMed]
  34. Ren, W.; Baig, A.; White, D.J.; Li, S.K. Characterization of cornified oral mucosa for iontophoretically enhanced delivery of chlorhexidine. Eur. J. Pharm. Biopharm. 2016, 99, 35–44. [Google Scholar] [CrossRef] [PubMed]
  35. Crevenna, R.; Burian, A.; Oesterreicher, Z.; Lackner, E.; Jäger, W.; Rezcicek, G.; Keilani, M.; Zeitlinger, M. Iontophoresis driven concentrations of topically administered diclofenac in skeletal muscle and blood of healthy subjects. Eur. J. Clin. Pharmacol. 2015, 71, 1359–1364. [Google Scholar] [CrossRef] [PubMed]
  36. Malinovskaja-Gomez, K.; Espuelas, S.; Garrido, M.J.; Hirvonen, J.; Laaksonen, T. Comparison of liposomal drug formulations for transdermal iontophoretic drug delivery. Eur. J. Pharm. Sci. 2017, 106, 294–301. [Google Scholar] [CrossRef] [PubMed]
  37. Viscusi, E.R.; Reynolds, L.; Chung, F.; Atkinson, L.E.; Khanna, S. Patient-controlled transdermal fentanyl hydrochloride vs intravenous morphine pump for postoperative pain: A randomized controlled trial. JAMA 2004, 291, 1333–1341. [Google Scholar] [CrossRef] [PubMed]
  38. Gratieri, T.; Kalia, Y.N. Targeted local simultaneous iontophoresis of chemotherapeutics for topical therapy of head and neck cancers. Int. J. Pharm. 2014, 460, 24–27. [Google Scholar] [CrossRef] [PubMed]
  39. Petrilli, R.; Eloy, J.O.; Saggioro, F.P.; Chesca, D.L.; de Souza, M.C.; Dias, M.V.; da Silva, L.L.; Lee, R.J.; Lopez, R.F. Skin cancer treatment effectiveness is improved by iontophoresis of EGFR-targeted liposomes containing 5-FU compared with subcutaneous injection. J. Control. Release 2018, 283, 151–162. [Google Scholar] [CrossRef] [PubMed]
  40. Eljarrat-Binstock, E.; Raiskup, F.; Frucht-Pery, J.; Domb, A.J. Hydrogel probe for iontophoresis drug delivery to the eye. J. Biomater. Sci. Polym. Ed. 2004, 15, 397–413. [Google Scholar] [CrossRef] [PubMed]
  41. Eljarrat-Binstock, E.; Raiskup, F.; Stepensky, D.; Domb, A.J.; Frucht-Pery, J. Delivery of gentamicin to the rabbit eye by drug-loaded hydrogel iontophoresis. Investig. Ophthalmol. Vis. Sci. 2004, 45, 2543–2548. [Google Scholar] [CrossRef] [PubMed]
  42. Frucht-Pery, J.; Mechoulam, H.; Siganos, C.S.; Ever-Hadani, P.; Shapiro, M.; Domb, A. Iontophoresis-gentamicin delivery into the rabbit cornea using a hydrogel delivery probe. Exp. Eye Res. 2004, 78, 745–749. [Google Scholar] [CrossRef]
  43. Day, R.E.; Megson, S.; Wood, D. Iontophoresis as a means of delivering antibiotics into allograft bone. J. Bone Jt. Surg. Br. 2005, 87, 1568–1574. [Google Scholar] [CrossRef] [PubMed][Green Version]
  44. Frucht-Pery, J.; Raiskup, F.; Mechoulam, H.; Shapiro, M.; Eljarrat-Binstock, E.; Domb, A. Iontophoretic treatment of experimental Pseudomonas keratitis in rabbit eyes using gentamicin-loaded hydrogels. Cornea 2006, 25, 1182–1186. [Google Scholar] [CrossRef] [PubMed]
  45. Toyoda, M.; Hama, S.; Ikeda, Y.; Nagasaki, Y.; Kogure, K. Anti-cancer vaccination by transdermal delivery of antigen peptide-loaded nanogels via iontophoresis. Int. J. Pharm. 2015, 483, 110–114. [Google Scholar] [CrossRef] [PubMed]
  46. Grossman, R.; Lee, D.A. Transscleral and transcorneal iontophoresis of ketoconazole in the rabbit eye. Ophthalmology 1989, 96, 724–729. [Google Scholar] [CrossRef]
  47. Lobo, S.; Yan, G. Improving the direct penetration into tissues underneath the skin with iontophoresis delivery of a ketoprofen cationic prodrug. Int. J. Pharm. 2018, 535, 228–236. [Google Scholar] [CrossRef] [PubMed]
  48. Wakita, R.; Oono, Y.; Oogami, S.; Hayashi, S.; Umino, M. The relation between epinephrine concentration and the anesthetic effect of lidocaine iontophoresis. Pain Pract. 2009, 9, 115–121. [Google Scholar] [CrossRef] [PubMed]
  49. Hu, L.; Silva, S.M.; Damaj, B.B.; Martin, R.; Michniak-Kohn, B.B. Transdermal and transbuccal drug delivery systems: Enhancement using iontophoretic and chemical approaches. Int. J. Pharm. 2011, 421, 53–62. [Google Scholar] [CrossRef] [PubMed]
  50. Wei, R.; Simon, L.; Hu, L.; Michniak-Kohn, B. Effects of iontophoresis and chemical enhancers on the transport of lidocaine and nicotine across the oral mucosa. Pharm. Res. 2012, 29, 961–971. [Google Scholar] [CrossRef] [PubMed]
  51. Ikeda, H.; Suda, H. Facilitatory effect of AC-iontophoresis of lidocaine hydrochloride on the permeability of human enamel and dentine in extracted teeth. Arch. Oral Biol. 2013, 58, 341–347. [Google Scholar] [CrossRef] [PubMed]
  52. Cubayachi, C.; Couto, R.O.; de Gaitani, C.M.; Pedrazzi, V.; Freitas, O.; Lopez, R.F. Needle-free buccal anesthesia using iontophoresis and amino amide salts combined in a mucoadhesive formulation. Colloids Surf. B Biointerfaces 2015, 136, 1193–1201. [Google Scholar] [CrossRef] [PubMed]
  53. Telo, I.; Tratta, E.; Guasconi, B.; Nicoli, S.; Pescina, S.; Govoni, P.; Santi, P.; Padula, C. In-vitro characterization of buccal iontophoresis: The case of sumatriptan succinate. Int. J. Pharm. 2016, 506, 420–428. [Google Scholar] [CrossRef] [PubMed]
  54. Sekijima, H.; Ehara, J.; Hanabata, Y.; Suzuki, T.; Kimura, S.; Lee, V.H.; Morimoto, Y.; Ueda, H. Characterization of ocular iontophoretic drug transport of ionic and nonionic compounds in isolated rabbit cornea and conjunctiva. Biol. Pharm. Bull. 2016, 39, 959–968. [Google Scholar] [CrossRef] [PubMed]
  55. Draper, D.O.; Coglianese, M.; Castel, C. Absorption of iontophoresis-driven 2% lidocaine with epinephrine in the tissues at 5 mm below the surface of the skin. J. Athl. Train. 2011, 46, 277–281. [Google Scholar] [CrossRef] [PubMed]
  56. Smitayothin, T.L.; Vongsavan, K.; Rirattanapong, P.; Kraivaphan, P.; Vongsavan, N.; Matthews, B. The iontophoresis of lignocaine with epinephrine into carious dentine for pain control during cavity preparation in human molars. Arch. Oral Biol. 2015, 60, 1104–1108. [Google Scholar] [CrossRef] [PubMed]
  57. Thongkukiatkun, W.; Vongsavan, K.; Kraivaphan, P.; Rirattanapong, P.; Vongsavan, N.; Matthews, B. Effects of the iontophoresis of lignocaine with epinephrine into exposed dentine on the sensitivity of the dentine in man. Arch. Oral Biol. 2015, 60, 1098–1103. [Google Scholar] [CrossRef] [PubMed]
  58. Puapichartdumrong, P.; Ikeda, H.; Suda, H. Facilitation of iontophoretic drug delivery through intact and caries-affected dentine. Int. Endod. J. 2003, 36, 674–681. [Google Scholar] [CrossRef] [PubMed]
  59. Mencucci, R.; Ambrosini, S.; Paladini, I.; Favuzza, E.; Boccalini, C.; Raugei, G.; Vannelli, G.B.; Marini, M. Early effects of corneal collagen cross-linking by iontophoresis in ex vivo human corneas. Graefes Arch. Clin. Exp. Ophthalmol. 2015, 253, 277–286. [Google Scholar] [CrossRef] [PubMed]
  60. Rong, S.; Wang, C.; Han, B.; Feng, P.; Lan, W.; Gao, Z.; Li, X.; Chen, W. Iontophoresis-assisted accelerated riboflavin/ultraviolet A scleral cross-linking: A potential treatment for pathologic myopia. Exp. Eye Res. 2017, 162, 37–47. [Google Scholar] [CrossRef] [PubMed]
  61. Jia, H.Z.; Pang, X.; Fan, Z.J.; Li, N.; Li, G.; Peng, X.J. Iontophoresis-assisted corneal crosslinking using 0.1% riboflavin for progressive keratoconus. Int. J. Ophthalmol. 2017, 10, 717–722. [Google Scholar] [CrossRef] [PubMed]
  62. Lombardo, M.; Giannini, D.; Lombardo, G.; Serrao, S. Randomized controlled trial comparing transepithelial corneal cross-linking using iontophoresis with the Dresden Protocol in progressive keratoconus. Ophthalmology 2017, 124, 804–812. [Google Scholar] [CrossRef] [PubMed]
  63. Lemos, C.N.; Cubayachi, C.; Dias, K.; Mendonça, J.N.; Lopes, N.P.; Furtado, N.A.J.C.; Lopez, R.F. Iontophoresis-stimulated silk fibroin films as a peptide delivery system for wound healing. Eur. J. Pharm. Biopharm. 2018, 128, 147–155. [Google Scholar] [CrossRef] [PubMed]
  64. Shirwaiker, R.A.; Wysk, R.A.; Kariyawasam, S.; Voigt, R.C.; Carrion, H.; Nembhard, H.B. Interdigitated silver-polymer-based antibacterial surface system activated by oligodynamic iontophoresis—An empirical characterization study. Biomed. Microdevices 2014, 16, 1–10. [Google Scholar] [CrossRef] [PubMed]
  65. Wagner, M.J.; Weil, T.M. Reduction of enamel acid solubility with electrophoretic fluoride applications. J. Dent. Res. 1966, 45, 1563. [Google Scholar] [CrossRef] [PubMed]
  66. Barbakow, F.H.; van der Merwe, E.H.M.; Scanes, S.G.; Retief, D.H.; Fatti, L.P. An in vivo evaluation of an iontophoretic technique for increasing the surface fluoride content in enamel. J. Dent. Assoc. S. Afr. 1973, 28, 624–629. [Google Scholar]
  67. Singal, P.; Gupta, R.; Pandit, N. 2% sodium fluoride-iontophoresis compared to a commercially available desensitizing agent. J. Periodontol. 2005, 76, 351–357. [Google Scholar] [CrossRef] [PubMed]
  68. Chen, L.J.; Meng, Q.F.; Chen, Y.M.; Smales, R.J.; Yip, K.H. Effect of fluoride iontophoresis on the microtensile bond strength between dentin and two adhesive systems. J. Dent. 2008, 36, 697–702. [Google Scholar] [CrossRef] [PubMed]
  69. Lee, Y.E.; Baek, H.J.; Choi, Y.H.; Jeong, S.H.; Park, Y.D.; Song, K.B. Comparison of remineralization effect of three topical fluoride regimens on enamel initial carious lesions. J. Dent. 2010, 38, 166–171. [Google Scholar] [CrossRef] [PubMed]
  70. Brahmbhatt, N.; Bhavsar, N.; Sahayata, V.; Acharya, A.; Kshatriya, P. A double blind controlled trial comparing three treatment modalities for dentin hypersensitivity. Med. Oral Patol. Oral Cir. Bucal 2012, 17, e483–e490. [Google Scholar] [CrossRef] [PubMed]
  71. Ren, W.; Baig, A.; Li, S.K. Passive and iontophoretic transport of fluorides across enamel in vitro. J. Pharm. Sci. 2014, 103, 1692–1700. [Google Scholar] [CrossRef] [PubMed]
  72. Kim, H.E.; Kim, B.I. Can the application of fluoride iontophoresis improve remineralisation of early caries lesions? Oral Health Prev. Dent. 2016, 14, 177–182. [Google Scholar] [CrossRef] [PubMed]
  73. Patil, A.R.; Varma, S.; Suragimath, G.; Abbayya, K.; Zope, S.A.; Kale, V. Comparative evaluation of efficacy of iontophoresis with 0.33% sodium fluoride gel and diode laser alone on occlusion of dentinal tubules. J. Clin. Diagn. Res. 2017, 11, ZC123–ZC126. [Google Scholar] [CrossRef] [PubMed]
  74. Tanaka, T.; Saito, A.; Watanabe, K.; Saeki, K.; Nakashima, H.; Maki, K. Preventive effects of iontophoresis on bovine enamel decalcification through enhancing uptake and transportation of fluoride—In vitro study. Pediatr. Dent. J. 2018, 28, 103–109. [Google Scholar] [CrossRef]
  75. Labala, S.; Jose, A.; Chawla, S.R.; Khan, M.S.; Bhatnagar, S.; Kulkarni, O.P.; Venuganti, V.V.K. Effective melanoma cancer suppression by iontophoretic co-delivery of STAT3 siRNA and imatinib using gold nanoparticles. Int. J. Pharm. 2017, 525, 407–417. [Google Scholar] [CrossRef] [PubMed]
  76. Sachdeva, V.; Kim, H.D.; Friden, P.M.; Banga, A.K. Iontophoresis mediated in vivo intradermal delivery of terbinafine hydrochloride. Int. J. Pharm. 2010, 393, 112–118. [Google Scholar] [CrossRef] [PubMed]
  77. Choi, T.B.; Lee, D.A. Transscleral and transcorneal iontophoresis of vancomycin in rabbit eyes. J. Ocul. Pharmacol. 1988, 4, 153–164. [Google Scholar] [CrossRef] [PubMed]
  78. Güngör, S.; Delgado-Charro, M.B.; Ruiz-Perez, B.; Schubert, W.; Isom, P.; Moslemy, P.; Patane, M.A.; Guy, R.H. Trans-scleral iontophoretic delivery of low molecular weight therapeutics. J. Control. Release 2010, 147, 225–231. [Google Scholar] [CrossRef] [PubMed][Green Version]
  79. Karpiński, T.M. Wpływ anestetyków lokalnych na odczyn zapalny. Influence of local anesthetics on inflammatoy reaction. Nowiny Lek. 2005, 74, 732–736. [Google Scholar]
  80. Rirattanapong, P.; Vongsavan, K.; Kraivaphan, P.; Vongsavan, N.; Matthews, B. Effect of the topical application of 50% lignocaine hydrochloride on the sensitivity of dentine in man. Arch. Oral Biol. 2013, 58, 1549–1555. [Google Scholar] [CrossRef] [PubMed]
  81. Ozawa, M.; Ikeda, H.; Suda, H. The effect of pulpward pressure on the response to 50% lidocaine (lignocaine) applied to exposed dentine in cats. Arch. Oral Biol. 2002, 47, 333–336. [Google Scholar] [CrossRef]
  82. Markowitz, K. Pretty painful: Why does tooth bleaching hurt? Med. Hypotheses 2010, 74, 835–840. [Google Scholar] [CrossRef] [PubMed]
  83. Saliba, S.A.; Teeter-Heyl, C.L.; McKeon, P.; Ingeroll, C.D.; Saliba, E.N. Effect of duration and amplitude of direct current when lidocaine is delivered by iontophoresis. Pharmaceutics 2011, 3, 923–931. [Google Scholar] [CrossRef] [PubMed]
  84. Power, I. Fentanyl HCl iontophoretic transdermal system (ITS): Clinical application of iontophoretic technology in the management of acute postoperative pain. Br. J. Anaesth. 2007, 98, 4–11. [Google Scholar] [CrossRef] [PubMed]
  85. Bonnet, F.; Eberhart, L.; Wennberg, E.; Dodds, S.J.; Van Bellinghen, L.; Annemans, L.; Kavanagh, S.; Choe, Y. Fentanyl HCl iontophoretic transdermal system versus morphine IV-PCA for postoperative pain management: Survey of healthcare provider opinion. Curr. Med. Res. Opin. 2009, 25, 293–301. [Google Scholar] [CrossRef] [PubMed]
  86. Patane, M.A.; Cohen, A.; From, S.; Torkildsen, G.; Welch, D.; Ousler, G.W., 3rd. Ocular iontophoresis of EGP-437 (dexamethasone phosphate) in dry eye patients: Results of a randomized clinical trial. Clin. Ophthalmol. 2011, 5, 633–643. [Google Scholar] [CrossRef] [PubMed]
  87. Cohen, A.E.; Assang, C.; Patane, M.A.; From, S.; Korenfeld, M.; Avion Study Investigators. Evaluation of dexamethasone phosphate delivered by ocular iontophoresis for treating noninfectious anterior uveitis. Ophthalmology 2012, 119, 66–73. [Google Scholar] [CrossRef] [PubMed]
  88. Patane, M.A.; Schubert, W.; Sanford, T.; Gee, R.; Burgos, M.; Isom, W.P.; Ruiz-Perez, B. Evaluation of ocular and general safety following repeated dosing of dexamethasone phosphate delivered by transscleral iontophoresis in rabbits. J. Ocul. Pharmacol. Ther. 2013, 29, 760–769. [Google Scholar] [CrossRef] [PubMed]
  89. Anderson, C.R.; Morris, R.L.; Boeh, S.D.; Panus, P.C.; Sembrowich, W.L. Effects of iontophoresis current magnitude and duration on dexamethasone deposition and localized drug retention. Phys. Ther. 2003, 83, 161–170. [Google Scholar] [PubMed]
  90. Wieckiewicz, M.; Boening, K.; Wiland, P.; Shiau, Y.Y.; Paradowska-Stolarz, A. Reported concepts for the treatment modalities and pain management of temporomandibular disorders. J. Headache Pain 2015, 16, 106. [Google Scholar] [CrossRef] [PubMed]
  91. Kogut, G.; Kwolek, A. Zaburzenia czynnościowe układu ruchowego narządu żucia-diagnostyka i leczenie. Rehabil. Med. 2006, 10, 41–48. [Google Scholar]
  92. Buescher, J.J. Temporomandibular joint disorders. Am. Fam. Phys. 2007, 76, 1477–1482. [Google Scholar]
  93. Wałach, A.; Pihut, M.; Loster, J. Charakterystyka zabiegów fizjoterapeutycznych stosowanych w leczeniu pacjentów z zaburzeniami czynnościowymi narządu żucia. Protet. Stomatol. 2006, 56, 274–281. [Google Scholar]
  94. Zimmermann-Górska, I.; Puszczewicz, M.; Białkowska-Puszczewicz, G. Ocena płynu stawowego jako podstawa stosowania preparatu Mobilat-żel w chorobach stawów. Reumatologia 1999, 37, 258–263. [Google Scholar]
  95. Arunkumar, S.; Shivakumar, H.N.; Narasimha Murthy, S. Effect of terpenes on transdermal iontophoretic delivery of diclofenac potassium under constant voltage. Pharm. Dev. Technol. 2017, 1–9. [Google Scholar] [CrossRef] [PubMed]
  96. Gianni, C. Update on antifungal therapy with terbinafine. G. Ital. Dermatol. Venereol. 2010, 145, 415–424. [Google Scholar] [PubMed]
  97. Wolinsky, J.B.; Colson, Y.L.; Grinstaff, M.W. Local drug delivery strategies for cancer treatment: Gels, nanoparticles, polymeric films, rods, and wafers. J. Control. Release 2012, 159, 14–26. [Google Scholar] [CrossRef] [PubMed][Green Version]
  98. Byrne, J.D.; Jajja, M.R.; O’Neill, A.T.; Bickford, L.R.; Keeler, A.W.; Hyder, N.; Wagner, K.; Deal, A.; Little, R.E.; Moffitt, R.A.; et al. Local iontophoretic administration of cytotoxic therapies to solid tumors. Sci. Transl. Med. 2015, 7, 273ra14. [Google Scholar] [CrossRef] [PubMed]
  99. Welch, M.L.; Grabski, W.J.; McCollough, M.L.; Skelton, H.G.; Smith, K.J.; Menon, P.A.; Anderson, L.L. 5-fluorouracil iontophoretic therapy for Bowen’s disease. J. Am. Acad. Dermatol. 1997, 36, 956–958. [Google Scholar] [CrossRef]
  100. Bacro, T.R.; Holladay, E.B.; Stith, M.J.; Maize, J.C.; Smith, C.M. Iontophoresis treatment of basal cell carcinoma with cisplatin: A case report. Cancer Detect. Prev. 2000, 24, 610–619. [Google Scholar] [PubMed]
  101. Zuckerman, J.E.; Davis, M.E. Clinical experiences with systemically administered siRNA-based therapeutics in cancer. Nat. Rev. Drug Discov. 2015, 14, 843–856. [Google Scholar] [CrossRef] [PubMed]
  102. Yu, H.; Pardoll, D.; Jove, R. STATs in cancer inflammation and immunity: A leading role for STAT3. Nat. Rev. Cancer 2009, 9, 798–809. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Scheme of iontophoretic device. Based on Dhote et al. [2], and Wanasathop and Li [7].
Figure 1. Scheme of iontophoretic device. Based on Dhote et al. [2], and Wanasathop and Li [7].
Pharmaceutics 10 00204 g001
Table 1. Summary of selected studies concerning iontophoretic application of drugs.
Table 1. Summary of selected studies concerning iontophoretic application of drugs.
DrugIontophoresis ConditionsTissueReferences
Acetylsalicylic acid5 mA/cm2, 10 minIn vivo rabbit eye[17]
Acetylsalicylic acid (Aspirin)0.06 mA, 10 minRat skin[11]
Acidulated phosphate fluoride0.4 mA, 4 minBovine enamel[18]
Acidulated phosphate fluoride0.2 mA, 4 minHuman teeth[19]
Aciclovir0.2 mA/cm2, 10 minIn vivo rat skin[20]
Aciclovir0.5 mA/cm2, 5 minPorcine eye[21]
Aciclovir prodrugs0.5 mA/cm2, 5 minPorcine eye[21]
Amikacin3.7–7.4 mA/cm2, 20 minIn vivo rabbit eye[22]
Amikacin sulphate0.5 mA/cm2, 2 hRabbit skin[23]
5-Aminolevulinic acid1–2 mA, 10 minIn vivo human skin[24]
Amoxicillin100, 200, 300 µA/cm2In vivo rabbit skin[25]
Cefuroxime100, 200, 300 µA/cm2In vivo rabbit skin[25]
Celecoxib0.1–0.5 mA/cm2, 25–300 minRat skin[26]
Ciprofloxacin0.8 mA, 10 minIn vivo rabbit cornea[27]
Ciprofloxacin hydrochloride6.25 mA/cm2, 5 minPorcine cornea and whole eye[28]
Cupral1.5 mA, 10 minHuman teeth root canals[29]
Curcumin with STAT3 siRNA0.47 mA/cm2, 4 hPorcine skin[30]
Dexamethasone0.36 mA/cm2, 10 and 20 minIn vivo human skin[31]
Dexamethasone4 mA, 15–30 minIn vivo human temporomandibular joint[32]
Dexamethasone5.1 mA/cm2, 4 minIn vivo rabbit cornea[33]
Dexamethasone1 mA/cm2, 180 minPorcine cornea[33]
Dexamethasone0.1 mA, 8 hBovine palate[34]
Diclofenac5 and 10 mA, 20 minIn vivo human muscle[35]
Diclofenac sodium0.5 mA/cm2, 8 hPorcine skin[36]
Ibuprofen0.06 mA, 10 minRat skin[11]
Indemethacin0.06 mA, 10 minRat skin[11]
Fentanyl hydrochloride10 minIn vivo human skin[37]
5-Fluorouracil1 mA/cm2, 10 and 20 minBovine buccal mucosa[38]
5-Fluorouracil0.5 mA/cm2, 15 min and 6 hPorcine skin[39]
Gentamicin sulfate2.5–5.1 mA/cm2, 1 and 2 minIn vivo rabbit cornea[40]
Gentamicin sulfate5.1 mA/cm2, 1 minIn vivo rabbit cornea[41]
Gentamicin sulfate0.51–3.1 mA/cm2, 1 minIn vivo rabbit cornea[42]
Gentamicin sulfate40 mA, 1, 5 and 10 minSheep and human bone[43]
Gentamicin sulfate0.8 and 2 mA/cm2, 1 minIn vivo rabbit cornea[44]
Gp100 peptide0.4 mA/cm2, 1 hIn vivo mouse melanoma[45]
Ketoconazole4–6 mA, 15 minRabbit eye[46]
Ketoprofen cationic prodrug0.2 mA, 6 hRat skin[47]
Leucovorin1 mA/cm2, 10 and 20 minBovine buccal mucosa[38]
Lidocaine1 mA, 10 minIn vivo human skin[48]
Lidocaine0.3 mA, 8 hPorcine buccal mucosa[49]
Lidocaine0.3 mA/cm2, 8 hPorcine buccal mucosa[50]
Lidocaine3 V, 1 kHz, 2–20 minHuman enamel/dentine[51]
Lidocaine1 mA/cm2, 1 hPorcine buccal mucosa[52]
Lidocaine0.5 mA/cm2, 6 hPorcine buccal mucosa[53]
Lidocaine0.5–5 mA/cm2 or 0.5–20 mA/cm2, 30 minRabbit cornea or rabbit conjunctiva[54]
Lignocaine with epinephrine1 mA, 10 minIn vivo human skin[48]
Lignocaine with epinephrine40 mA, 10.5 minIn vivo human skin[55]
Lignocaine with epinephrine0.2 mA, 2–14 minHuman dentine[56]
Lignocaine with epinephrine0.12 mA, 90 sHuman dentine[57]
Metronidazole0.05 mA, 10 minHuman dentine[58]
Naproxen sodium0.05 mA, 10 minHuman dentine[58]
Potassium iodide1.5 mA, 10 minHuman teeth root canals[29]
Riboflavin1 mA, 5 min + UVA irradianceHuman cornea[59]
Riboflavin10 minIn vivo rabbit eye[60]
Riboflavin1 mA, 5 minIn vivo human eye[61]
Riboflavin-5-phosphate1 mA, 5 minIn vivo human cornea[62]
Silk fibroin with neurotensin0.2 mA/cm2, 30 minMacrophages[63]
Silver-polymer-based surface1.5–15 µA, 30 minBacterial strains[64]
Sodium fluoride0.5–0.6 mA, 30 sRat enamel[65]
Sodium fluoride10 mA, 2–3.3 minHuman enamel[66]
Sodium fluoride0.5 mA, 2 minIn vivo human teeth[67]
Sodium fluoride0.5 mA, 5 minHuman dentine[68]
Sodium fluoride0.4 mA, 4 minBovine enamel[18]
Sodium fluoride0.2 mA, 4 minBovine enamel[69]
Sodium fluoride0.5 mA, 2 minIn vivo human teeth[70]
Sodium fluoride0.2 mA, 4 minHuman teeth[19]
Sodium fluoride0.1 mA, 8 hBovine enamel[71]
Sodium fluoride0.1 mA, 8 hBovine palate[34]
Sodium fluoride0.3 mA, 4 min, for 5 daysBovine enamel[72]
Sodium fluoride1.5 mA, 3 minHuman dentine[73]
Sodium fluoride0.5 mA, 3 min
0.5 mA, 5 min
0.5 mA, 10 min
Bovine enamel[74]
Sodium salicylate0.05 mA, 10 minHuman dentine[58]
Sodium salicylate0.1 mA, 8 hBovine palate[34]
STAT3 siRNA with imatinib mesylate0.5 mA/cm2, 2 hIn vivo mouse melanoma[75]
Terbinafine hydrochloride0.25 mA, 10, 15 and 20 minIn vivo rat skin[76]
Vancomycin0.5–3.5 mA, 10 minRabbit eye[77]
Vancomycin2.55–10.2 mA/cm2, 120 minRabbit sclera[78]

Share and Cite

MDPI and ACS Style

Karpiński, T.M. Selected Medicines Used in Iontophoresis. Pharmaceutics 2018, 10, 204.

AMA Style

Karpiński TM. Selected Medicines Used in Iontophoresis. Pharmaceutics. 2018; 10(4):204.

Chicago/Turabian Style

Karpiński, Tomasz M. 2018. "Selected Medicines Used in Iontophoresis" Pharmaceutics 10, no. 4: 204.

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop