Indexed with PubMed and Science Citation Index (E) 
Users online: 3856 
     Home | Feedback | Login 
About Current Issue Archive Ahead of print Search Instructions Online Submission Subscribe What's New Contact  
  Navigate here 
 # Next article
 # Previous article 
 # Table of Contents
 Resource links
 #  Similar in PUBMED
    Search Pubmed for
    Search in Google Scholar for
  Related articles
 #  Article in PDF (92 KB)
 #  Citation Manager
 #  Access Statistics
 #  Reader Comments
 #  Email Alert *
 #  Add to My List *
* Registration required (free)  

  In this article
 #  Abstract
 #  Introduction
 #  Material and Methods
 #  Observations and...
 #  Discussion
 #  Source(s) of support
 #  References

 Article Access Statistics
    PDF Downloaded272    
    Comments [Add]    
    Cited by others 2    

Recommend this journal

Year : 2003  |  Volume : 69  |  Issue : 4  |  Page : 271--273

Topical lincomycin gel in acne vulgaris: A multicentric placebo controlled study

Wallace Pharmaceutical Ltd., Mumbai

Correspondence Address:
Wallace Pharmaceutical Pvt. Ltd., A-101/102, Floral Deck Plaza, Off Central MIDC Road, Andheri (E), Mumbai - 400073

  #  Abstract

Introduction: Acne vulgaris is commonly treated with topical antibacterials. We evaluated lincomycin gel, a new topical formulation for mild to moderate acne. Material and Methods: A multicentric, randomized, double blind, placebo controlled, clinical trial was conducted with lincomycin hydrochloride in 2% gel form in 200 patients with grade II and grade III acne. The severity of acne lesions was noted at baseline and after 4 weeks. Results: About 70% cases in the study group showed a good to excellent response, which was significantly more as compared to 23% in the placebo group. The frequency and severity of adverse reactions in the two groups were similar. Conclusion: Lincomycin hydrochloride gel is an effective and safe treatment option for mild to moderate acne vulgaris.

How to cite this article:
Sharma A D, Gupte P D, Sundaram M, Janaki V R, Rege V L, Bilimoria F E, Arora J. Topical lincomycin gel in acne vulgaris: A multicentric placebo controlled study . Indian J Dermatol Venereol Leprol 2003;69:271-3

How to cite this URL:
Sharma A D, Gupte P D, Sundaram M, Janaki V R, Rege V L, Bilimoria F E, Arora J. Topical lincomycin gel in acne vulgaris: A multicentric placebo controlled study . Indian J Dermatol Venereol Leprol [serial online] 2003 [cited 2020 May 28];69:271-3. Available from: http://www.ijdvl.com/text.asp?2003/69/4/271/4991

  ::   Introduction Top

Topical antibacterials used in acne vulgaris act against Propionibacterium acnes. They also have a mild indirect effect on comedogenesis and anti-inflammatory activity by impeding neutrophil chemotaxis. Erythromycin and clindamycin are currently the two most commonly used antibiotics. Many cases reported to be resistant to erythromycin have surfaced[1] and hence lincosamides like clindamycin have gained acceptance. Lincomycin is another antibacterial from this group that has potent activity against Propionibacterium acnes.[2]

  ::   Material and Methods Top

After the initial clearance through toxicological studies like acute and chronic dermal toxicity studies using different animal models,[3] a multicentric clinical trial on lincomycin hydrochloride 2% gel (Lynx; Wallace Pharma Pvt. Ltd., India) was initiated to study its efficacy and safety in acne vulgaris. This trial was conducted at five different centres approved by the Drug Controller General of India.

Two hundred and sixteen patients of either sex over 12 years of age with clinically confirmed and graded acne vulgaris lesions were included. These patients were enrolled from the dermatological OPD of the above centers after taking a valid consent. Patients with a known history of hypersensitivity to lincosamides were excluded from the study. Ambulatory patients with Grade II and Grade III acne vulgaris were included in the study. The grading was done using the Pillsbury grading scale.[4] Photographs of the acne lesions were taken on day 1, 7, 14, 21 and 28 to assess the efficacy of the drug.

Of the patients enrolled at each centre about half of them were assigned randomly to the drug treatment group and the other half to the placebo group. As per their group, patients were told to apply either 2% lincomycin gel or the placebo gel (the same gel formulation without lincomycin) over acne lesions twice daily after washing the face with soap and water. No other concomitant anti-acne therapy was allowed. The number, size and the severity of inflammation of the lesions were noted separately for each body region at the initial visit and every week thereafter for 4 weeks. Double blinding was carried out by the study monitor.

The response to the treatment was assessed as follows:
Excellent response : Complete healing of acne lesions clinically.
Good response : 50% or more reduction in number of acne lesions.
Fair response : 25%-50% reduction in number of acne lesions
Poor response : No response, flare-up of lesions, or less than 25% reduction in the number of acne lesions.

Patients were monitored for adverse drug reactions during the study period. The data was statistically analyzed using t-test and chi-square statistical tests. The proportion of patients with a reduction in the number of lesions, i.e. improvement or cure of acne, and with flare up of disease depending on the baseline lesions, evaluated on clinical basis are presented as percentages.

  ::   Observations and results Top

All in all 200 patients completed the study, 100 belonging to the placebo group and 100 to the lincomycin group. The two groups were comparable in terms of the age and sex distribution of patients, duration of disease and total number of acne lesions at baseline [Table-1].

After the treatment was initiated, the number of lesions started reducing from the first week onwards in both the groups, but the reduction was 57.04% in the lincomycin treated group, which was significantly more as compared to 31.28% in the placebo group [Table-2].

Upon global assessment, in the lincomycin group 70% of the cases showed more than 50% reduction in acne lesions, which was significantly more than the corresponding figure of 23% in the placebo treated group [Table-3].

The adverse reactions were mostly mild and self limiting; common ones were itching, burning, dryness, erythema, scaling and pigmentation. Itching, erythema and pigmentation were slightly more common in the placebo group than in the lincomycin group [Table-4].
The drop out rate in the lincomycin in group was 6% wheras that in the placebo group was 10%. No patient dropped out on account of severe adverse event.

  ::   Discussion Top

Acne is a multifactorial disorder. Suppression of P. acnes with antibiotic therapy correlates with clinical improvement.[5],[6] Antibiotics like erythromycin and clindamycin, and more recently azithromycin, are most frequently used to treat acne vulgaris.[7] Topical preparations for acne are available in various formulations, the gel formulation being most commonly preferred since it is cosmetically acceptable and best suited for oily skin. Topically applied lincomycin has good tissue penetration with potent activity against P. acnes (MIC < 0.1-1.6 mcg/ml).[14] By its action on P. acnes, lincomycin eliminates the production of free fatty acids and other local irritating enzymes produced by bacteria. Further, it may have some immunomodulating effect in reducing inflammation.[15] These attributes of lincomycin prompted the development of its topical formulation, lincomycin hydrochloride as a 2% gel (Lynx ), for acne.

In the present study, the resolution of acne lesions was quite satisfactory; good response (reduction in severity of acne by 50% or more at the end of 4 weeks) was seen in 70% of patients as compared to only 23% of the placebo treated group. Such a response in 70% of patients with grade II and grade III acne is suggestive of noteworthy anti-acne properties of 2% lincomycin gel.

The adverse effects observed were localized skin reactions like itching, erythema, scaling and pigmentation. They were mild in intensity and self limiting. They occurred more commonly in the placebo group, one possible explanation being a flaring up of the disease. No case of contact sensitization or severe allergic skin reaction was noted. Almost all topical antibiotics are associated with some minor skin irritation. This adverse effect may be influenced by the vehicle used.[8]

The emergence of erythromycin resistance in cutaneous propionibacteria was first reported in USA in the late 1970's in patients treated with topical erythromycin or clindamycin.[9] The good response to topical lincomycin in this study could be due to the fact that P. acnes has developed resistance against commonly used antibiotics such as erythromycin, whereas lincomycin still remains effective against these strains of P. acnes. However, this needs to be established by in vitro and in vivo comparision of lincomycin with erthromycin. Moreover, cross resistance between lincomycin and erythromycin is not observed,[10] and for lincomycin it develops in a stepwise manner.[11] In a clinical study by Eady et al, one in every four acne patients attending the clinic carried erythromycin-resistant propionibacteria on the facial skin.[9],[12] The development of resistance in acne can be limited by the rational use of topical antibiotics and restricting oral antibiotic therapy.[9],[13]

  ::   Source(s) of support Top
Initiated and financed by Wallace Pharma Pvt. Ltd., India.

  #   References Top

1.Eady EA, Cove JH. Erythromycin resistant propionibacteria in antibiotic treated acne patients: Association with therapeutic failure. Br J Dermatol 1989;121:51-7.  Back to cited text no. 1    
2.Lincosamides. In: Drugs facts and comparisons. In: Hebel SK, Kastrup EK, et al, editors. Facts and comparisons. 56th ed. Missouri: 2002. p. 1399-400.  Back to cited text no. 2    
3.Pillsbury DM, Shelley B, Kligman AM. Dermatology. Philadelphia: WB Saunders; 1956. p. 810.  Back to cited text no. 3    
4.Johnson BA, Nunley JR. Use of systemic agents in the treatment of acne vulgaris. Am Fam Phys 2000;62:1823-30.  Back to cited text no. 4  [PUBMED]  
5.Wyatt EL, Sutter SH, Drake LA. Dermatological pharmacology. In: Hardman JG, Limbird LE, editors. Goodman & Gilman's The pharmacological basis of therapeutics. New York: McGraw Hill; 1996. p. 1605-16.  Back to cited text no. 5    
6.Fernandez-Obregon AC. Azithromycin for the treatment of acne. Int J Dermatol 2000;39:45-50.  Back to cited text no. 6  [PUBMED]  [FULLTEXT]
7.Russell J. Topical therapy for acne. Am Fam Phys 2000;61:357-65.  Back to cited text no. 7    
8.Eady EA, Parmery MR, Ross JI, Cove JH, Cunlife WI. Effects of benzoyl peroxide and erythromycin alone and in combination against antibiotic-sensitive and -resistant skin bacteria from acne patients. Br J Dermatol 1994;131:331-6.  Back to cited text no. 8    
9.Clapper WE, Meade GH, Stewart DB. The susceptibility of certain bacteria to lincomycin as related to attainable serum levels in human adults. Am J Med Sci 1964;247:274-7.  Back to cited text no. 9  [PUBMED]  
10.Lincomycin hydrochloride. In: Branch RA, Coley KC, Holiman TD, et al, editors. Mosby's Gen Rx-Drug information. 9th ed. Missouri: Mosby Publications; 1999. p.1333-4.  Back to cited text no. 10    
11.Eady EA, Jones CE, Cove JH, et al. Antibiotic resistant propionobacterium in acne: Need for policies to modify antibiotic usage. BMJ 1993;306:555-6.  Back to cited text no. 11    
12.Strauss JS, Pochi PE, Downing DT. Acne: Perspectives. J Invest Dermatol 1974;62:321-5.  Back to cited text no. 12    
13.Herrel WE. Lincomycin. Chicago: Modern Scientific Publications; 1969.  Back to cited text no. 13    
14.Kucers A, Crowe S, Grayson ML, Hoy J. The use of antibiotics. 4th ed. Oxford: Butterworth Heinemann; 1989. p. 587-605.  Back to cited text no. 14    


Print this article  Email this article


Online since 15th March '04
Published by Wolters Kluwer - Medknow