Automatic Patch Adhesion Testing using Arduino
Ramya P1, Padmapriya B2, Poornachandra S3, Arumugaraja M4
1Assistant Professor, SNS College of Engineering, Coimbatore, Tamil Nadu
2Assosiate Professor, PSG College of Technology, Coimbatore, Tamil Nadu
3Professor, Excel Engineering College, Namakkal Dt.
4Scholar, PSG College of Technology, Coimbatore, Tamil Nadu
*Corresponding Author E-mail: ramya.ece.snsce@gmail.com, bpp.bme@psgtech.ac.in, pcmed8@gmail.com, mail2me.raja@gmail.com
ABSTRACT:
In order to study and evaluate the suitability method of predicting the long term adhesion properties of patches to human skin is the biggest challenges in the medical sectors. adhesion to the skin is strictly linked to the efficiently and safety of the therapeutic treatment, now-a- days numerous report of in vivo adhesion lacking are still addressed to regulatory agencies. In real time health care system involving human skin an adhesion patch need to be integrated into diagnostic device. In medical field it is efficient to provide a patch adhesive capacity. Our motive is to develop the patch adhesion tester to determine adhesiveness of the patch. When the patch is given to the proposed tester then the measured values of the given patch will be displayed.
KEYWORDS: Patch adhesive tester, Bio medical instruments, Embedded medical instruments.
1. INTRODUCTION:
Grip is the security quality estimation of a covering to a substrate. At the point when a cement is clung to a thing or surface, various physical, mechanical and substance powers become possibly the most important factor, which may affect one another.
Assurance of the disappointment point can be basic for the last utilization of the material and the glue. There are a substantial number of various glue items, which require diverse testing strategies to describe the properties of the material. [10] Some precedents incorporate substrates, stick, creams, gels, paints and varnishes and holding of various materials together in layers, which all require distinctive cement test techniques.
The disappointment point can be basic for the last utilization of the materials, contingent upon the last item they have been intended for. Tests should likewise be possible at various temperatures to reproduce certifiable use for the materials. Material attributes can change at high or low temperatures because of development and withdrawal.
Attachment testing is regularly connected with glues, tape, sealants, overlays, hardware, beautifiers, restorative gadget bundling, general bundling seal quality and applications where bond quality estimation is basic for research and quality control applications. Stud pull covering grip testing, for example, is an extremely regular test utilized in miniaturized scale electronic coatings or different types of "thin film" application on unbending substrates.
2. LITERATURE REVIEW:
Fix testing is an entrenched strategy for diagnosing contact allergy– a postponed kind of excessive touchiness (type IV response). Patients with a history and clinical picture of contact dermatitis are re-presented to the speculated allergens under controlled conditions to confirm the analysis. [32,35] Likewise testing patients with hand (dyshidrotic, hyperkeratotic), arm, face or leg skin inflammation (stasis dermatitis), testing of different sorts of dermatitis (atopic, seborrheic dermatitis, nummular skin inflammation), incorporating patients with interminable psoriasis, vulval disarranges or medication responses, is in some cases demonstrated, particularly when they are hard-headed to endorsed treatment and the dermatologist presumes contact hypersensitivity to recommended topical remarks and their vehicles. [8,9] Apart from its utilization to affirm a speculated unfavorably susceptible contact dermatitis, the fix test method can likewise be utilized before prescribing elective icaments, healthy skin items, beauty care products, gloves, and so on in a specific patient.[30] If the patient does not respond to the choices tried, it is far-fetched that the person will respond to the items in normal use.
Later, frequently cited, rules are exhibited by Malten et al. [1], Fregert [2] and Bandmann and Wohn [3]. A few investigations (e.g. [4– 6]) have appeared nitty gritty fix testing is useful for patients and enhance their personal satisfaction (QoL). [8] However, it has additionally been guaranteed that irregular fix testing with a standard arrangement ought to be debilitated because of low pretest likelihood [27]. When performing patch testing it must be recalled that the fix test is a natural incitement test and in that capacity the result is subject to different variables including the test framework and test material, the organic/practical status of the tried individual, and the capable dermatologist. [37]
GENTAG creates about undetectable dispensable skin patches. GENTAG has sensors inserted into the patches, yet in addition utilizes iontophoresis to convey sedates through the epidermis without a needle. [16] Their patches incorporate a Fever fix, Fitness checking, Skincare (measures UV presentation), Diabetes observing, and tranquilize conveyance for an assortment of drugs. GENTAG likewise has Radar Responsive (RR) labels for geo area data and physiological well being. [17] Their RR labels were tried with the USA country protection, however are currently sold for following competitors at major wearing occasions, Alzheimer's patients, firefighters, and little youngsters. The best capacity about GENTAG's patches are that they require no battery – totally detached technology. [18]
2.1 Standardization
The main fix tests as indicated by present standards were completed in 1895 yet were gone before by some primer analyses. Amid the most recent couple of decades much exertion has been put into institutionalization of allergens, vehicles, focuses, fix test materials, tapes, and the scoring of test responses, and the strategy today is viewed as precise and reliable. [21] A progression of papers have exhibited great propagation of fix test results. Institutionalization has encouraged examinations of contact hypersensitivity recurrence in and between facilities, land regions, and regions with different degrees of industrialization yet a few inquiries still remain, particularly concerning the perusing and scoring of test reactions. [22]
2.2 Bio availability:
Bio accessibility to acquire ideal bio accessibility can impact the accompanying five factors: Intrinsic infiltration limit fixation, portion vehicle impediment of fix test framework and tape presentation time since it is alluring to evacuate all test strips in the meantime – more often than not at day 2 (48 h) – four variables remain and can be changed and improved by the makers of fix test materials and allergen arrangements and by the dermatologist in charge of the testing. [20] The entrance limit can rely on the salts utilized; for instance, there is a major distinction between the infiltration of nickel accomplished by nickel sulfate and nickel chloride [24]. The higher infiltration of nickel from the chloride is likely clarified by the segment skin/vehicle of the salts when connected in a similar vehicle in equimolar fixation and under impediment.
3. BLOCK DIAGRAM:
Fig 1: Block diagram of Patch Adhesive Testing
Patches:
Transdermal fixes and mortars (fix) speak to settled delayed discharge dose frames. Regardless of whether acceptable grip to the skin is entirely connected to the viability and security of the remedial treatment, these days various reports of in viva 'attachment lacking' are as yet routed to administrative agencies.[30] The cement properties of a fix ought to be described thinking about I) the capacity to frame a bond with the surface of another material on brief contact and under light weight (tack); ii) the obstruction of the glue to stream (shear bond); and iii) the power required to strip away a fix from a surface (strip attachment).
Fig 2:Mechanical Block diagram of Patch Adhesive Testing
4. EXPERIMENTATION AND RESULT:
4.1 Methodology:
In this composition, the most broadly utilized techniques to gauge cement properties amid advancement thinks about are portrayed, alongside the quality control of patches. The impact of detailing factors on fix glue properties and their conceivable relationship inside the wearable skin patches are ending up increasingly more present inside the wearable market. They can be utilized for games, sedate conveyance, or patient monitoring.[12] Skin patches are perfect since they can be covered up under apparel, don't meddle with development and accordingly can record increasingly exact information. Wearable patches are not removable patches for apparel or wraps that embrace the skin, rather, they are stick glues that might possibly contain a drug or sensor.
At the point when the framework is reset, the program introduces the circuit and it shows that the framework is prepared. The DC engine introduces to its position when the framework is reset. By putting the fix to introductory position, we need to start the test. When the test is started, the engine begins running and we need to pull the arm the other way. Concerning the heap, the sensor estimates the scope of load and it is reflected in the processor. The processor changes over the information into advanced shape and shows it in the LCD show.
The sensor estimates the precision of the adhesiveness concerning the heap connected, for instance, 102.01gms.
Fig 4: System Initialization
Fig 5: Output value of the adhesiveness is displayed in LED display
Specifications Table
|
Subject area |
Biomedical |
|
More specific subject area |
Biomedical Patch adhesive testing |
|
Type of data |
Values |
|
How data was acquired |
Using Arduino patch adhesiveness is calculated |
|
Data format |
Raw |
|
Experimental factors |
Patch adhesiveness can be tested using Arduino board |
|
Experimental features |
Patch adhesive tester measures the value of given patch and the output value is displayed. |
|
Data source location |
Anywhere |
|
Data accessibility |
Accessible for all those who are using this tester in medical field |
Value of the data:
· Patch testing is a settled technique for diagnosing contact allergy– a deferred sort of extreme touchiness.
· Transdermal fixes and sedated mortars (fix) speak to entrenched delayed discharge measurements frames.
· The cement properties of a fix ought to be described thinking about I) the capacity to shape a bond with the surface of another material on brief contact and under light weight (tack); ii) the obstruction of the cement to stream (shear attachment); and iii) the power required to strip away a fix from a surface (strip grip).
Data:
Attachment testing is regularly connected with glues, tape, sealants, covers, gadgets, beautifying agents, medicinal gadget bundling, general bundling seal quality and applications where bond quality estimation is basic for research and quality control applications. Stud pull covering attachment testing, for example, is an exceptionally basic test utilized in miniaturized scale electronic coatings or different types of "thin film" application on inflexible substrates.
In therapeutic field it is proficient to give a fix cement limit consequently we built up the fix bond analyzer to decide adhesiveness of the fix. At the point when the fix is given to the proposed analyzer then the deliberate estimations of the given fix will be shown and we can without much of a stretch distinguish the adhesiveness of the fix.
5. CONCLUSION:
Here we presume that progressively medicinal services framework including human skin an attachment fix has been coordinated into symptomatic gadget. In restorative field it is productive to give a fix glue limit subsequently we built up the fix attachment analyzer to decide adhesiveness of the fix. At the point when the fix is given to the proposed analyzer then the deliberate estimations of the given fix will be shown and we can undoubtedly distinguish the adhesiveness of the fix.
6. REFERENCES:
1. Malten KE, Nater JP, van Ketel WG (1976) Patch testing guidelines. Dekker and van de Vegt, Nijmegen
2. Fregert S (1981) Manual of contact dermatitis, 2nd edn. Munksgaard, Copenhagen
3. Rajagopolan R, Anderson R (1997) Impact of patch testing on dermatology-specific quality of life in patients with allergic contact dermatitis. Am J Contact Dermat 8:215–221
4. Thomson KF, Wilkinson SM, Sommer S, Pollock B (2002) Eczema: quality of life by body site and the effect of patch testing. Br J Dermatol 146:627–630
5. Woo PN, Hay IC, Ormerod AS (2003) An audit of the value of patch testing and its effect on quality of life. Contact Dermatitis 48:244–247
6. Van der Valk PGM, Devos SA, Coenraads P-J (2003) Evidence-based diagnosis in patch testing. Contact Dermatitis 48:121–125
7. Mowad CM (2006) Patch testing: pitfalls and performance. CurrOpin Allergy ClinImmunol 6:340–344
8. Jadassohn J (1896) Zur Kenntnisder ikamentösen Dermatosen, Verhandlungen der Deutschen Dermatologischen Gesellschaft. Fünfter Congress, Raz, 1895. Braunmuller, Vienna, p 106
9. Foussereau J (1984) History of epicutaneous testing: the blotting-paper and other methods. Contact Dermatitis 11:219–223
10. Fischer TI, Hansen J, Kreilgård B, Maibach HI (1989) The science of patch test standardization. Immunol Allergy Clin North Am 9:417–443
11. Belsito DV, Storrs FJ, Taylor JS, Marks JG Jr, Adams RM, Rietschel RL, Jordan WP, Emmett EA (1992) Reproducibility of patch tests: a United States multi-centre study. Am J Contact Dermat 3:193–200
12. Breit R, Agathos M (1992) Qualitätskontrolle der Epikutantestung – Reproduzierbarkeitim Rechts-Links-Vergleich. Hautarzt 43:417–421
13. Bousema MT, Geursen AM, van Joost T (1991) High reproducibility of patch tests. J Am Acad Dermatol 24:322–323
14. Lachapelle JM, Antoine JL (1989) Problems raised by the simultaneous reproducibility of positive allergic patch test reactions in man. J Am Acad Dermatol 21:850–854
15. Machácková J, Seda O (1991) Reproducibility of patch tests. J Am Acad Dermatol 25:732–733
16. Lindelöf B (1990) A left versus right side comparative study of Finn Chamber™ patch tests in 220 consecutive patients. Contact Dermatitis 22:288–289
17. Stransky L, Krasteva M (1992) A left versus right side comparative study of Finn Chamber patch tests in consecutive patients with contact sensitization. Dermatosen 40:158–159
18. Brasch J, Henseler T, Aberer W, Bäuerle G, Frosch PJ, Fuchs T, Fünfstück V, Kaiser G, Lischka GG, Pilz B, Sauer C, Schaller J, Scheuer B, Szliska C (1994) Reproducibility of patch tests. A multicenter study of synchronous left-versus right-sided patch tests by the German Contact Dermatitis Research Group. J Am Acad Dermatol 31:584–591
19. Gollhausen R, Przybilla B, Ring J (1989) Reproducibility of patch test results: comparison of True test and Finn Chamber test. In: Frosch PJ, Dooms-Goossens A, Lachapelle JM, Rycroft RJ, Scheper RJ (eds) Current topics in contact dermatitis. Springer, Berlin, pp 524–529
20. Lachapelle J-M, Bruynzeel DP, Ducombs G, Hannuksela M, Ring J, White IR, Wilkinson J, Fischer T, Billberg K (1988) European multicenter study of the True test™. Contact Dermatitis 19:91–97
21. Ruhnek-Forsbeck M, Fischer T, ing B, Pettersson L, Stenberg B, Strand A, Sundberg K, Svensson L, Wahlberg JE, Widström L, Wrangsjö K, Billberg K (1988) Comparative multi-center study with True test™ and Finn Chamber® patch test methods in eight Swedish hospitals. ActaDermVenereol (Stockh) 68:123–128
22. Stenberg B, Billberg K, Fischer T, Nordin L, Pettersson L, Ruhnek-Forsbeck M, Sundberg K, Swanbeck G, Svensson L, Wahlberg JE, Widström L, Wrangsjö K (1989) Swedish multicenter study with True test, panel 2. In: Frosch PJ, Dooms-Goossens A, Lachapelle JM, Rycroft RJ, Scheper RJ (eds) Current topics in contact dermatitis. Springer, Berlin, pp 518–523
23. Wilkinson JD, Bruynzeel DP, Ducombs G, Frosch PJ, Gunnarsson Y, Hannuksela M, Ring J, Shaw S, White IR (1990) European multicenter study of TRUE test, panel 2. Contact Dermatitis 22:218–225
24. Rajashri R. Kulkarni, Dipti G. Phadtare. The Microneedle Patches: An Innovative Approach. Asian J. Pharm. Tech. 2015; Vol. 5(4): 195-200.
25. Schiessl C, Wolber C, Strohal R (2004) Reproducibility of patch tests: comparison of identical test allergens from different commercial sources. Contact Dermatitis 50:27–30
26. Kintu Patel, SankalpPatel,Samir K. Shah. Daily dose, in a Dot. Asian J. Pharm. Res. 2017; 7(4): 225-229.
27. Katta Manogna, T.N. Shilpa, . Development of Medicated Topical Patches in Transdermal drug delivery system. Research J. Pharm. and Tech. 2018; 11(1): 397-404.
28. Brasch J, Szliska C, Grabbe J (1997) More positive patch test reactions with larger test chambers? Contact Dermatitis 37:118–120
29. Gefeller O, Phahlberg A, Geier J, Brasch J, Uter W (1999) The association between size of test chamber and patch test reaction: a statistical reanalysis. Contact Dermatitis 40:14–18
30. Arijit Das, Sibaji Ghosh, Sudip Das, Biplab Kr. Dey, Tarun Kanti Ghosh. Formulation and In Vitro Evaluation of Transdermal Patches of Metformin Hydrochloride Using Hydrophilic and Hydrophobic Polymer Complex. Research J. Pharm. and Tech. 4(4): April 2011; Page 561-565.
31. Dooms-Goossens A, Degree H (1983) Contact allergy to petrolatums I. Sensitizing capacity of different brands of yellow and white petrolatums. Contact Dermatitis 9:175–185
32. Dey BK, Kar PK, Nath LK. Formulation Design, Preparation and In vitro – In vivo Evaluation of Propranolol Hydrochloride Transdermal Patches using Hydrophilic and Hydrophobic Polymer complex. Research J. Pharm. and Tech. 2(1): Jan.-Mar. 2009; Page 155-160
33. Fischer T, Maibach H (1989) Easier patch testing with TRUE test. J Am AcadDermatol 20:447–453
34. Magnusson B, Blohm S-G, Fregert S, Hjorth N, Høvding G, Pirilä V, Skog E (1966) Routine patch testing II. ActaDermVenereol (Stockh) 46:153–158
35. Suresh V Kulkarni, Ranjit Kumar P, Nikunj Patel, Ramesh B, Someshwara Rao B, Ashok Kumar P. Development and Evaluation of Diltiazem Hydrochloride Transdermal Patches by Using Glycerol and Castor Oil as Plasticizers. Research J. Pharm. and Tech.3 (3): July-Sept. 2010; Page 905-909.
36. Benezra C, Andanson J, Chabeau C, Ducombs G, Foussereau J, Lachapelle JM, Lacroix M, Martin P (1978) Concentrations of patch test allergens: are we comparing the same things? Contact Dermatitis 4:103–105
37. Suja C., Ramasamy C., Narayanacharyulu R. Development and Evaluation of Lisinopril Transdermal Patches. Research J. Pharm. and Tech. 4(8): August 2011; Page 1260-1264.
38. Akhil Gupta, Anuj Mittal ,Alok Kumar Gupta. Colon Targeted Drug Delivery Systems – A Review. Asian J. Pharm. Res. 1(2): April-June 2011; Page 25-33.
39. Wahlberg JE (1996) Nickel: the search for alternative, optimal and non-irritant patch test preparations. Assessments based on laser Doppler flowmetry. Skin Res Technol 2: 136–141
40. Asma Afroz, Md. Asaduzzaman, Md. Rezowanur Rahman, S.M. Ashraful Islam. Development and Evaluation of Muco-Adhesive Ciprofloxacin Bi-Layer Tablet for Extended Drug Release. Asian J. Pharm. Res. 1(3): July-Sept. 2011; Page 64-68
41. Design and Evaluation of Terbutaline Sulphate Buccal Patch Wani MS, Dehghan MH, Mahendra Kumar C, Polshettiwar SA, Yadav VB. Research J. Pharm. and Tech. 2(1): Jan.-Mar. 2009; Page 86-90.
42. Daecke C, Schaller S, Schaller J, Goos M (1993) Contact urticaria from acrylic acid in Fixomull tape. Contact Dermatitis 29:216–217.
Received on 20.12.2018 Modified on 11.02.2019
Accepted on 16.03.2019 © RJPT All right reserved
Research J. Pharm. and Tech. 2019; 12(4):1769-1772.
DOI: 10.5958/0974-360X.2019.00296.8