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J Adv Periodontol Implant Dent. 11(2):69-76. doi: 10.15171/japid.2019.012

Research Article

Efficacy of 2% ibuprofen subgingival irrigation as an adjunct to non-surgical therapy in the treatment of chronic periodontitis: A randomized controlled, split-mouth, clinical trial

Amirhossein Farahmand 1, Ferena Sayar 2, * , Zohreh Omidali 3 ORCID logo, Mahsa Soleimani 1 ORCID logo, Bahareh Jafarzadeh Esfahani 3 ORCID logo
1Department of Periodontics, Faculty of Dentistry, Islamic Azad University, Tehran, Iran
2Department of Periodontics, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran
3Dentist, Private Practice
*Corresponding Author: E-mail: sayar_ferna@yahoo.com

Abstract

Background

Pharmacological factors, such as ibuprofen, released topically in the periodontal pocket modulate the host response and enhance the influence of non-surgical periodontal treatment.

Methods

In this double-blind, randomized, split-mouth, clinical trial, 38 outpatients with mild to moderate chronic periodontitis were enrolled by applying the simple random sampling method. They had at least one tooth with a periodontal pocket depth of >4 mm in each quadrant and had undergone phase I of periodontal treatment one week after scaling and root planing (SRP). The parameters of clinical periodontal evaluation, including probing pocket depth (PPD), clinical attachment level (CAL), plaque index (PI), and bleeding index (BI), were measured. In addition, two mandibular molar teeth in one quadrant were randomly nominated for subgingival irrigation with 0.5 mL of 2% ibuprofen or placebo mouthwash. The measurements were repeated after at least one week for three months.

Results

Thirty-four individuals (18 women and 16 men), with an age range of 28‒36 years, were evaluated for three months. Moreover, periodontal clinical parameters were assessed within three months. There was a significant improvement in pocket depth (PD) and clinical attachment level (CAL) readings after 12 weeks in both groups (paired t-test). On comparing, the group with scaling and root planing (SRP) + ibuprofen showed more favorable results than the group with SRP + placebo (P<0.05). There were significant improvements in PI and BI in both groups; the differences between the two groups were significant (P<0.05).

Conclusion

The mouthwashes containing ibuprofen might reduce the symptoms of periodontal disease and might be used as an adjunct in the healing process.

Keywords: Chronic periodontitis, ibuprofen, irrigation, non-surgical, periodontal therapy

Copyright

© 2019 The Author(s).
This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Introduction

Chronic periodontitis is an infectious disease marked by periodontal pocket formation that results in the inflammation and destruction of periodontal tissues. 1 It is well known that periodontal disease mainly progresses due to bacterial infection; however, the initiation and progression of the disease can vary among objects in terms of genetic predisposition, systemic status, and environmental effects. 2-4 There is a large body of studies showing that both surgical and non-surgical periodontal treatments are effective against periodontitis by eliminating pathogenic dental plaque and calculus. 5 Non-surgical periodontal treatment reduces pocket depth (PD) and increases clinical attachment level (CAL) to some extent; 6,7 however, it cannot fill the bony defect. 8 In addition, some patients do not respond to traditional periodontal treatment, 9 or exhibit a highly elevated susceptibility to periodontal disease. 10 Assessment of the mechanisms underlying these events has shown that the immune response of patients seems to play a critical role in the extension and the manifestation of periodontal diseases. 11,12 The host modulation treatment is to restore the balance of pro-inflammatory or destructive mediators and anti-inflammatory or protective mediators to that seen in healthy patients. Host modulation treatment is a method believed to decrease tissue damage and maintain or even restore inflammatory tissues by altering host response agents. 13 However, non-steroidal anti-inflammatory drugs (NSAIDs) are known as inhibitors of the formation of Prostanoids (including prostaglandins and thromboxane), and this has been the source of much interest in the inhibitors of the host immune response to periodontal disease. Prostanoids are produced during the activation of the cyclooxygenase pathway to periodontal disease, which is associated with tissue destruction and bone loss. Investigators suggest that selective NSAIDs (COX-2 inhibitors) might reduce the bone loss associated with periodontitis; 14 additionally, host modulation using various therapeutic agents targeting the manipulation of the inflammatory pathway has been proposed as an adjunctive treatment with conventional periodontal therapy. 15-18 The latest survey determined that the use of NSAIDs in combination with mechanical periodontal therapy improved bone maintenance in treating patients with periodontal diseases. 19 Of all the various combinations of these, such as flurbiprofen, ibuprofen is readily absorbed through the gingival tissues. Moreover, the development of local NSAID formulations (e.g., gels, toothpaste, and rinses) with daily employment appears to be of particular interest. These products might result in a greater decrease in the harmful systemic influences of non-selective NSAIDs in the long-term host modulation of periodontitis-susceptible subjects (20). Furthermore, studies have shown that prostaglandin production inhibitors, including non-steroidal anti-inflammatory drugs (NSAIDs), can influence this phase of bone loss in periodontal disease. 21 The current study aimed to evaluate the clinical effectiveness of subgingival irrigation with 2% ibuprofen as an adjunct to scaling and root planing (SRP) in patients with chronic periodontitis.


Methods

Study Protocol and Selection of Patients

This study was carried out as a single-center, examiner-blinded, randomized, split-mouth clinical trial, with a two-arm, parallel-group design, in three months. This study was undertaken to assess the clinical application of a combination plus locally applied ibuprofen (2%) mouthwash (made in the Faculty of Pharmaceutical Sciences, Islamic Azad University, Tehran, Iran) in combination with SRP versus SRP + placebo mouthwash. The clinical measures of periodontal disease were evaluated in patients attending the Department of Periodontics, Faculty of Dentistry, Islamic Azad University, Tehran, Iran. Thirty-eight patients of both genders, aged 28‒35 years, were selected, who were diagnosed with mild to moderate chronic periodontitis conforming to the 1999 Classification of Periodontal Diseases and Conditions with a probing depth >4 mm (Academy of Periodontology in 1999). 22

Inclusion Criteria

The inclusion criteria consisted of a confirmed diagnosis of early moderate chronic periodontitis, at least two residual areas with a probing pocket depth (PPD) of >4 mm in two opposite quadrants, and CAL of ≥1‒2 mm, at least 20 remaining teeth with two teeth in every mandibular quadrant. The clinical periodontal parameters were determined and recorded at baseline within seven days for 12 weeks in the selected teeth, at six locations in each tooth, using a periodontal probe (Williams Probe, Hu-Friedy, USA) by two calibrated masked investigators (periodontists). Pocket depths were defined as the distance from the gingival margin to the bottom of the pocket, and CAL was defined as the distance from the cementoenamel junction (CEJ) to the base of the pocket. PI was measured using a Silness & Löe index. 23,24 BoP was evaluated through visual inspection 30 seconds after probing according to Carter & Barnes (score 0: no bleeding after probing; score 1: a single separate bleeding point becomes visible after probing). 25

Exclusion Criteria

Patients with the following conditions were excluded: known hypersensitivity to the components of the formulation, those with systemic disease, pregnant and breastfeeding women, those undergoing orthodontic treatment, those with numerous dental bridges, those taking anti-inflammatory drugs, antibiotics, or immunosuppressive medicines in the latest three months, those wearing a partial denture, those with numerous carious lesions, those habitually smoking, and those with a history of periodontal surgery.

Intervention

The periodontal clinical parameters were noted at the baseline. All the subjects received full-mouth SRP and polishing at baseline. Oral care instructions were given that included tooth brushing for two minutes twice a day with the modified Bass technique with a soft-bristled brush (soft toothbrushes protect gums and gingival margin against damage). Moreover, the subjects were randomly assigned to two groups of equal size. Group A received SRP combined with ibuprofen mouthwash; group B subjects were treated with SRP in combination with a placebo mouthwash. The periodontal pocket depth was defined at six areas per tooth; also, the left and right mandibular quadrants were allocated. In both categories, the mouthwashes (2% ibuprofen or placebo) were applied to all the periodontal pockets (pocket depth of >4 mm), using an insulin syringe with the blunt needle inserted into the bottom of the periodontal pocket; 0.5 mL of 2% ibuprofen mouth rinse was applied to each surface (distal, mid, and mesial) of the lower first and second molars. Then, all the pre- and post-treatment periodontal clinical parameters were registered by two investigators who were masked to the type of medication, while another clinician delivered the respective operations to both groups. The patients were recalled at 7-day intervals within three months to examine periodontal clinical parameters.

Sample Size

Conforming to previous examinations, the sample size evaluation was based on identifying changes in the principal consequences of periodontal disease measurements ‒ probing depth (PD) from the baseline to the end of the follow-up. The sample size of the study was calculated using “two-sample t-test sample size calculation” tab of MINITAB software, considering α=0.05, β=0.05, a mean difference of 1.65, and pooled standard deviation=1.4. Finally, 17 subjects were necessary for each group.

Randomization and Blinding

Randomization was carried out by one of the investigators who did not have a role in the treatment of the subjects. Eligible participants who proved their ongoing commitment to the study were block-randomized to treatment in a double-blinded manner, implemented as block randomization with a 4:1 allocation. All the mouthwashes were placed in identical bottles and labeled A or B. Each participant picked one symbol from a box to decide his/her sequence of the use of mouthwashes. The randomized order of mouthwash use during the entire clinical study was controlled by a calibrated examiner. Moreover, before initiating the investigation, an examiner (a periodontist) was trained in a calibration process twice until it reduced the researcher reliability. The examiner was calibrated for one week before the start of the experiments. Periodontal assessments were performed by a single calibrated examiner. The examiner evaluated the subjects on two occasions: at baseline and after two days. Calibration was validated, as 90% of the readings were reproduced within a 1.0-mm difference.

Statistical Analysis

SPSS 21.0 was used for the analysis of data. Student’s t-test was applied for intragroup comparisons of the paired samples. ANOVA was employed for intergroup comparison using the mean variance values of the clinical periodontal parameters (plaque index or bleeding scores) on the first day to the last appointment within three months. P-values<0.05 were considered as statistically significant.


Results

The mean age of the subjects was 28‒35 (31.0±3.2) years in both groups. Gender distribution included 18 women and 16 men in the two groups (Figure 1). The initial analysis evaluated intention-to-treat and involved all the subjects. Two patients did not record back for the first follow-up appointment, and two patients from each group failed to return for follow-up visits after the second visit. Therefore, they were excluded from the current study. At baseline, no significant differentiation was observed between the groups in any of the clinical periodontal parameters. After thorough SRP, followed by routine maintenance, the rate of plaque control in all the patients proved adequate; during the examination, plaque development decreased with significant differences between the two groups. Also, dental plaque deposits were minimal, with significant differences between the two groups. Statistically, a significant difference was found in PI between the ibuprofen and placebo mouthwashes after 12 weeks. However, the PI score was significantly higher in the ibuprofen mouthwash group compared to the placebo group at the three-month interval (P<0.05) (Table 1). The BI and PD significantly decreased in the ibuprofen group compared to the placebo group after 6 and 12 weeks (P<0.05; Table 2 & Table 3). However, the CAL was significantly different only after 12 weeks in the ibuprofen group compared to the placebo group (P<0.05) (Table 4). The data were further analyzed to define variations in the distribution of the CAL before and after treatment. The ibuprofen group exhibited a significantly higher CAL than the placebo group. In the ibuprofen group, the percentage of patients with a gain in CAL between 1.5 and 2 mm was 0% versus 17% at the 12-week interval, indicating an improved CAL in the ibuprofen group compared to the placebo group. All the subjects tolerated the medicine well without any complications or adverse reactions. The soft tissues healed within normal limits, and no significant differences were observed.

japid-11-69-g001
Figure 1. CONSORT 2010 Flow Diagram

Table 1. The effect of both treatments on the mean values of plaque index (PI) among the study groups at baseline, 0, 1 and 3 months after treatment
Plaque index Ibuprofen group Placebo group
Baseline 0.1±0.730.1± 0.74
6 weeks 0.43±0.030.49±0.02
12weeks 0.38±0.010.43±0.02
p.value P<0.0001
Table 2. The effect of both treatments on the mean values of Bleeding index (BI) among the study groups at baseline, 0, 1 and 3 months after treatment
Bleeding on probing Ibuprofen group Placebo group
Baseline 0.97±0.680.98±0.67
6 weeks 0.63±0.050.85±0.09
12weeks 0.50± 0.060.73±0.08
P-value P<0.0001
Table 3. The effect of both treatments on the mean values of pocket depth (PD) among the study groups at baseline, 0, 1 and 3 months after treatment
Pocket depth Ibuprofen group Placebo group
Baseline 4.60±0.864.61± 0.83
6 weeks 3.40±0.153.86 ±0.15
12weeks 2.70± 0.183.32±0.21
P-value P<0.0001
Table 4. The effect of both treatments on the mean values of Clinical attachment level (CAL) among the study groups at baseline, 0, 1 and 3 months after treatment
CAL Ibuprofen group Placebo group
Baseline 4.82±0.494.82±0.51
6 weeks 3.56±0.103.92±0. 12
12weeks 2.90±0.163.50 ±0.23
P-value P<0.0001

Discussion

The present clinical study showed that COX-1 inhibitors might significantly decrease periodontal diseases and the healing of periodontal parameters compared to placebo mouthwash. On the other hand, the results showed the clinical efficacy of 2% ibuprofen mouthwash as an adjunct to periodontal debridement for the treatment of periodontal diseases. Furthermore, several studies have indicated the effect of the host response on the periodontium by blocking and modulating periodontal disease development. 26 In the present study, the changes in periodontal parameters after subgingival irrigation with ibuprofen led to a significant reduction in bleeding on probing at baseline and after 15, 30, 45, 60, 75, and 90 days.

Consistent with the present study, Yewey et al 27 showed in beagle dogs that the application of a biodegradable subgingival delivery system for flurbiprofen resulted in a significant reduction in gingival inflammation. In another study, it was shown the statistically significant recovery in the gingival situation of the subjects with the use of a flurbiprofen gel as an adjunct to SRP as correlated with oral prophylaxis or flurbiprofen gel only. 28 Paolantonio reported that subgingival irrigation with 1% ASA in patients with periodontal disease resulted in a reduction in subclinical inflammation of the periodontal pockets. 29 Paquette et al 30 showed that at the 90-day interval, the reduction in BoP was highly significant compared with the two other groups.

Srinivas et al 31 reported the most considerable decrease in BoP with ketoprofen, which was significant, but it was found to be ineffective in reducing the pocket depth and CAL when ketoprofen gel was used. Vogel et al 32 showed that the local steroidal drug significantly prevented gingival inflammation, whereas the systematically applied non-steroidal drug had no apparent effect, also concluding that there was no significant effect on gingival crevicular fluid and BoP. Furthermore, Corry and Moran 33 suggested the use of strips of polymethacrylate cement as a delivery vehicle for the sustained release of NSAIDs, such as indomethacin, as an essential system for treating periodontal diseases. 33 However, the decrease in gingival inflammation might be attributed to the lowered plaque toxicity, interference with the subgingival plaque maturation, or possibly washing away unattached plaque. 34-36

Furthermore, the present study showed a decrease in the clinical parameters of probing depth and clinical attachment levels. Del Puente et al 37 showed that the use of NSAIDs in cases with adult periodontitis resulted in less attachment loss. Funosas et al 38 showed that intra-crevicular application of 1% ASA and 2% ketoprofen gel as an adjunct to periodontal treatment in patients with chronic periodontitis could significantly reduce probing depths. In another study, the maximum PD reduction was observed in a few deep sites (7 mm) in the SRP‒loxoprofen group compared to the SRP‒placebo group. 39 However, several studies have shown that subgingival irrigation decreased mean probing depths by only one mm. 40,41 Nonetheless, several studies exhibited an even less reduction. 42-46 In other words, In root planing with irrigation therapy, probing pocket depths decreased up to 2 to 3 mm. 44,47-49 Therefore, if probing pocket depth decrease is required, root planing is indicated.

Furthermore, different agents that might influence drug delivery, such as calculus, irrigator head design, and irrigation pressure, have also been investigated. 50 The present study also showed a significant change in the plaque index score at 90 days. On the contrary, Johanson et al 51 showed that the drug has no significant effect on the plaque or bleeding index scores. Naprosyn might increase healing following the removal of microbial plaque; however, this drug does not suppress the inflammation-inducing properties of plaque, Naprosyn might increase recovery following plaque removal. 51 It is noteworthy that subgingival irrigation with medicines decreased plaque indices but failed to reduce the symptoms of inflammation; 48-55 however, when root planing was also employed, there were fewer bleeding spots. 44,49,50,56,57 Although the reduction in the inflammation of gingiva might have been due to lowered plaque toxicity, interference with the subgingival plaque maturation, or possibly removal of unattached plaque. 34-38

Farahmand et al 58 reported that the Ibuprofen gel, as an adjunct to SRP, might open up new horizons in the management of periodontal therapy and could be used to supplement the treatment to determine the inflammatory process and clinical signs of the disease more rapidly. Batool et al 59 injected 1.5% chlorhexidine and ibuprofen into the periodontal pockets in an experimental periodontitis mouse model and reported a reduction in inflammation and an improvement in periodontal wound healing through inflammatory cell scoring after treatment. Furthermore, another study showed that electrospun polycaprolactone scaffold functionalized with ibuprofen significantly improved the clinical attachment, reduced inflammation-induced bone loss, efficiently and differentially controlled inflammatory and migratory gingival cell reaction, and probably promoted periodontal regeneration. 60 That is why topical use is a valid alternative for completing the treatment of periodontal disease.

Local forms used in dentistry involve mouthrinses, supra- and subgingival irrigation, and subgingival devices. Subgingival or intra-crevicular tools improve the time that the active element remains within the periodontal pocket, thus assuring a longer delivery time. Various subgingival devices, as vehicles for delivering NSAIDs, have been studied, such as the subgingival irritation tools described by Paolantonio et al. 29

By improving oral hygiene habits plus periodontal therapy, a mechanical plaque control treatment on bacterial plaque could be reached, after which the anti-inflammatory action of NSAIDs could be applied in perfect treatment during a healing process. Furthermore, as there are many inflammatory mediators correlated with the host response in periodontal disease, it is necessary to clarify what drug offers the several appropriate effects on bone, soft tissues, and even upon some inflammatory mediators. However, the topically administered NSAIDs protocols employed in this investigation did not alter the plaque index more than the placebo did.

As the infectious factors that produce and improve the inflammatory process need to be reduced to enable NSAID anti-inflammatory activity, the plaque score might be expected to be a variable independent of NSAIDs employment, and more related to mechanical debridement, basic therapy, or changes in the patient's brushing method. However, it should be pointed out that some primary data imply that irrigation with high concentrations of substantive drugs might enhance the efficiency of root planing. Therefore, further research is needed to show the efficacy of this treatment modification. Hence, subgingival irrigation might be useful when root planing is less effective due to anatomical or other factors. Nevertheless, it becomes evident that the major failure of irrigation treatment is the immediate removal of subgingivally placed medications.


Conclusion

Mechanical periodontal therapy is the most effective procedure for the treatment of chronic periodontitis. Now, it seems the use of topical medications might reduce the manifestations of periodontal disease, as well as mouthwashes containing ibuprofen.


Authors’ Contributions

AF and MS designed and performed the experiments AF and FS conceived of the idea. AF, FS, and ZO implemented the study and performed data analysis. AF and BJE prepared the manuscript. MS edited the manuscript.


Competing Interests

The authors declare no conflict(s) of interest related to the publication of this work.


Ethics Approval

The research protocol was reviewed and approved by the Ethics Committee (code of ethics: 2161) of the Faculty of Dentistry, and also registered in the Iranian Registry of Clinical Trials (code: IRCT2014050917587N4) and the clinicaltrials.gov (code: NCT02538237). The study procedure conforms to the principles outlined in the Declaration of Helsinki on human medical experimentation. Verbal and written informed consent was obtained from all the participants.


References

  1. Savage A, Eaton KA, Moles DR, Needleman me. A systematic review of definitions of periodontitis and methods that have been used to identify this disease. J Clin Periodontol 2009 Jun; 36(6):458-67. [ Google Scholar]
  2. Havemose-Poulsen A, Sørensen LK, Bendtzen K, Holmstrup P. Polymorphisms within the IL-1 gene cluster: effects on cytokine profiles in peripheral blood and whole blood cell cultures of patients with aggressive periodontitis, juvenile idiopathic arthritis, and rheumatoid arthritis. J Periodontol 2007; 78:475-92. [ Google Scholar]
  3. Löe H. Periodontal disease The sixth complication of diabetes mellitus. Diabetes Care 1993; 16:329-34. [ Google Scholar]
  4. Tomar SL, Asma S. Smoking-attributable periodontitis in the United States: findings from NHANES III National Health and Nutrition Examination Survey. J Periodontol 2000; 71:743-51. [ Google Scholar]
  5. Cobb CM. Clinical significance of non-surgical periodontal therapy: an evidence-based perspective of scaling and root planing. J Clin Periodontol 2002; 29 Suppl 2:6-16. [ Google Scholar]
  6. Vidal F, Cordovil I, Figueredo CM, Fischer RG. Non-surgical periodontal treatment reduces cardiovascular risk in refractory hypertensive patients: a pilot study. J Clin Periodontol 2013; 40(7):681-687. [ Google Scholar]
  7. Vergnes JN, Canceill T, Vinel A, Laurencin-Dalicieux S, Maupas-Schwalm F, Blasco-Baque V, Hanaire H, Arrive E, Rigalleau V, Nabet C. The effects of periodontal treatment on diabetic patients: the DIAPERIO randomized controlled trial. J Clin Periodontol 2018; 45(10):1150-1163. [ Google Scholar]
  8. Bertl K, Parllaku A, Pandis N, Buhlin K, Klinge B, Stavropoulos A. The effect of local and systemic statin use as an adjunct to non-surgical and surgical periodontal therapy-a systematic review and meta-analysis. J Dent 2017; 67:18-28. [ Google Scholar]
  9. Haffajee AD, Socransky SS, Ebersole JL. Survival analysis of periodontal sites before and after periodontal therapy. J Clin Periodontol 1985; 12:553-67. [ Google Scholar]
  10. Giannobile WV, Braun TM, Caplis AK, DoucetteStamm L, Duff GW, Kornman KS. Patient stratification for preventive care in dentistry. J Dent Res 2013; 92:694-701. [ Google Scholar]
  11. Kornman KS, Page RC, Tonetti MS. The host response to the microbial challenge in periodontitis: assembling the players. Periodontol 2000 1997; 14:33-53. [ Google Scholar]
  12. Page RC. The role of inflammatory mediators in the pathogenesis of periodontal disease. J Periodontal Res 1991; 26(3 Pt 2):230-42. [ Google Scholar]
  13. 2. ShaluBathla, Host Modulatory Therapy, In Periodontics Revisited, 1st Edition, 292-295, 2011.
  14. Protective effects of etoricoxib, a selective inhibitor of cyclooxygenase-2, in experimental periodontitis in rats. J Periodontal Res 2005; 40(3):208-11. [ Google Scholar]
  15. Ohm K, Albers HK, Lisboa BP. Measurement of eight prostaglandins in human gingival and periodontal disease using high pressure liquid chromatography and radioimmunoassay. J Periodontal Res 1984; 19:501-511. [ Google Scholar]
  16. Abramson MM, Wolff LF, Offenbacher S, Aeppli DM, Hardie ND, Friedman HM. Flurbiprofen effect on gingival crevicular fluid prostaglandin and thromboxane levels in humans. J Periodontal Res 1992 Sep; 27(5):539-43. [ Google Scholar]
  17. Jeffcoat MK, Reddy MS, Haigh S, Buchanan W, Doyle MJ, Meredith MP, Nelson SL, Goodale MB, Wehmeyer KR. A comparison of topical ketorolac, systemic flurbiprofen, and placebo for the inhibition of bone loss in adult periodontitis. J Periodontol 1995 May; 66(5):329-38. [ Google Scholar]
  18. Offenbacher S, Williams RC, Jeffcoat MK, Howell TH, Odle BM, Smith MA, Hall CM, Johnson HG, Goldhaber P. Effects of NSAIDs on beagle crevicular cyclooxygenase metabolites and periodontal bone loss. J Periodontal Res 1992 May; 27(3):207-13. [ Google Scholar]
  19. Reddy MS etal. Periodontal host modulation with antiproteinase, anti-inflammatory and bone sparing agents A systematic review. Ann Periodontol 2003; 8(1):12-37. [ Google Scholar]
  20. Salvi GE, N N. P Lang The Effects of Non-Steroidal Anti-Inflammatory Drugs [Selective and Non-Selective] on the Treatment of Periodontal Diseases. Curr Pharm Des 2005; 11(14):1757-69. [ Google Scholar]
  21. Howell TH, Fiorellini J, Weber HP, Williams RC. Effect of the NSAID piroxicam, topically administered, on the development of gingivitis in beagle dogs. J Periodontal Res 1991; 26(3 Pt 1):180-3. [ Google Scholar]
  22. Armitage GC. Development of a classification system for periodontal diseases and conditions. Ann Periodontol 1999; 4(1):1-6. [ Google Scholar]
  23. Silness J, Loe H. Periodontal disease in pregnancy II Correlation between oral hygiene and periodontal condition. Acta Odontol Scand 1964; 22:121-35. [ Google Scholar]
  24. O’Leary TJ, Drake RB, Naylor JE. The plaque control record. J Periodontol 1972; 43(1):38. [ Google Scholar]
  25. Carter HG, Barnes GP. The gingival bleeding index. J Periodontol 1974; 45(11):801-5. [ Google Scholar]
  26. Page R, Offenbacher S, Schroeder HE, Seymour GJ, Kornman KS. Advances in the pathogenesis of periodontitis: Summary of developments, clinical implications and future directions. Periodontol 2000 1997; 14:216-248. [ Google Scholar]
  27. Yewey GL, Tipton AJ, Dunn RL, Manardi EM, McEnvoy RM. Evaluation of biodegradable subgingival delivery system for Flurbiprofen. J Dent Res 1991; 70:324. [ Google Scholar]
  28. Deshpande NC, Bhat KM, Bhat GS, Deshpande AN. Randomized, controlled clinical study to evaluate efficacy of novel indigenously designed controlled release flurbiprofen gel system for management of periodontal diseases. Contemp Clin Dent 2013 Jan; 4(1):32-6. [ Google Scholar]
  29. Paolantonio M , Fanali S , Di Genova S . Effetto di irrigazioni subgengivali con acetilsalicilato sul numero di leucociti polimorfonucleati in tasche parodontali di media profondita. Minerva Stomatol 1995; 44:265-271. [ Google Scholar]
  30. Paquette DW, Lawrence HP, Maynor GB, Wilder R, Binder TA, Troullos E. Pharmacodynamic effects of ketoprofen on crevicular fluid prostanoids in adult periodontitis. J Clin Periodontol 2000; 27:558-66. [ Google Scholar]
  31. Srinivas M, Medaiah S, Girish S, Anil M, Pai J, Walvekar A. The effect of ketoprofen in chronic periodontitis: A clinical double-blind study. J Indian Soc Periodontol 2011 Jul; 15(3):255-9. [ Google Scholar]
  32. Vogel RI, Copper SA, Schneider LG, Goteiner D. The effects of topical steroidal and systemic nonsteroidal anti-inflammatory drugs on experimental gingivitis in man. J Periodontol 1984 Apr; 55(4):247-51. [ Google Scholar]
  33. Corry D, Moran J. Assessment of acrylic bone cement as a local delivery vehicle for the application of non-steroidal anti-inflammatory drugs. Biomaterials 1998; 19:1295-1301. [ Google Scholar]
  34. Flemmig TF, Newman MG, Doherty F. Supragingival irrigation with 006% chlorhexidine in naturally occurring gingivitis I 6-month clinical observations. J Periodontol 1990; 61:112-117. [ Google Scholar]
  35. Derdivanis JP, Bushmaker S, Dagenais F. Effects of a mouthwash in an irrigating device on accumulation and maturation of dental plaque. J Periodontol 1978; 49:81-84. [ Google Scholar]
  36. Fine DH, Letizia OJ, Mandel ID. The effect of rinsing with Listerine antiseptic on the properties of developing dental plaque. J Clin Periodontol 1985; 12:660-666. [ Google Scholar]
  37. Del Puente A, Shlossman M, Arevalo A, Knowler W, Genco R. Relationship of rheumatoid arthritis and periodontal disease [Abstr2064]. J Dent Res 1988; 67(Spec. Issue):371. [ Google Scholar]
  38. Funosas ER, Escovich L, Maestri L. The use of topical subgingival gels of non-steroidal anti-inflammatory drugs (NSAIDs) as an adjunct to non-surgical management of chronic periodontitis. Acta Odontol Latinoam 2009; 22(3):215-9. [ Google Scholar]
  39. Pinho Mde N, Pereira LB, de Souza SL, Palioto DB, Grisi MF, Novaes AB Jr, Taba M Jr. Short-term effect of COX-2 selective inhibitor as an adjunct for the treatment of periodontal disease: a clinical double-blind study in humans. Braz Dent J 2008; 19(4):323-8. [ Google Scholar]
  40. Haskel E, Esquenasi J, Yussim L. Effects of subgingival chlorhexidine irrigation in chronic moderate periodontitis. J Periodontol 1986; 57:305-310. [ Google Scholar]
  41. Lazzaro AJ, Bissada NF. Clinical and microbiologic changes following the irrigation of periodontal pockets with metronidazole or stannous fluoride. Periodontol Case Rep 1989; 1:12-19. [ Google Scholar]
  42. Soh LL, Newman HN, Strahan JD. Effects of subgingival chlorhexidine irrigation on periodontal inflammation. J Clin Periodontol 1982; 9:66-74. [ Google Scholar]
  43. Lander PE, Newcomb GM, Seymour G, Powell N. The antimicrobial and clinical effects of a single subgingival irrigation of chlorhexidine in advanced periodontal lesions. J Clin Periodontol 1986; 13:74-80. [ Google Scholar]
  44. Wennstro¨m JL, Dahle´n G, Gro¨ndahl K, Heijl L. Periodic subgingival antimicrobial irrigation of pockets II Microbiologic and radiographical observations. J Clin Periodontol 1987; 14:573-580. [ Google Scholar]
  45. Vignarajah S, Newman HN, Bulman J. Pulsated jet subgingival irrigation with 01% chlorhexidine, simplified oral hygiene and chronic periodontitis. J Clin Periodontol 1989; 16:365-370. [ Google Scholar]
  46. Fine JB, Harper DS, Gordon JM, Hovliaras CA, Charles CH. Short-term microbiological and clinical effects of subgingival irrigation with an antimicrobial mouthrinse. J Periodontol 1994; 65:30-36. [ Google Scholar]
  47. Southard S, Drisko CL, Killoy WJ. The effects of2% chlorhexidine digluconate irrigation on the clinical parameters and level of Bacteroides gingivalis in periodontal pockets. J Periodontol 1989; 60:302-309. [ Google Scholar]
  48. MacAlpine R, Magnusson I, Kiger R, Crigger M, Garrett S, Egelberg J. Antimicrobial irrigation of deep pockets to supplement oral hygiene instruction and root debridement I Bi-weekly irrigation. J Clin Periodontol 1985; 12:568-577. [ Google Scholar]
  49. Braatz L, Garrett S, Claffey N, Egelberg J. Antimicrobial irrigation of deep pockets to supplement nonsurgical periodontal therapy II Daily irrigation. J Clin Periodontol 1985; 12:630-638. [ Google Scholar]
  50. Larner JR, Greenstein G. Effect of calculus and irrigation tip design depth of subgingival irrigation. Int J Periodontics Restorative Dent 1993; 13:288-297. [ Google Scholar]
  51. Johanson R H. Assessment of efficacy of a non-steroidal anti-inflamatory drug, Naprosyn, in the treatment of gingivitis. Journal of Periodontal Research 1990; 25:230—235. [ Google Scholar]
  52. Silverstein L, Bissada N, Manouchehr-Pour M, Greenwell H. Clinical and microbiologic effects of local tetracycline irrigation on periodontitis. J Periodontol 1988; 59:301-305. [ Google Scholar]
  53. Listgarten M, Grossberg D, Schwimer AV, Gaffer A. Effect of subgingival irrigation with tetrapotassium peroxydiphosphate on scaled and untreated periodontal pockets. J Periodontol 1989; 60:4-11. [ Google Scholar]
  54. Vignarajah S, Newman HN, Bulman J. Pulsated jet subgingival irrigation with 01% chlorhexidine, simplified oral hygiene and chronic periodontitis. J Clin Periodontol 1989; 16:365-370. [ Google Scholar]
  55. Fine JB, Harper DS, Gordon JM, Hovliaras CA, Charles CH. Short-term microbiological and clinical effects of subgingival irrigation with an antimicrobial mouthrinse. J Periodontol 1994; 65:30-36. [ Google Scholar]
  56. Wan Yusof W, Newman HN, Strahan JD. Subgingival metronidazole in dialysis tubing and subgingival chlorhexidine irrigation in the control of chronic inflammatory periodontal disease. J Clin Periodontol 1984; 11:166-175. [ Google Scholar]
  57. Watts EA, Newman HN. Clinical effects on chronic periodontitis of a simplified system of oral hygiene including subgingival pulsated jet irrigation with chlorhexidine. J Clin Periodontol 1986; 13:666-670. [ Google Scholar]
  58. Amirhossein Farahmand, Ferena Sayar, Bahareh Jafarzadeh Esfahani. Clinical Efficacy of Subgingivally Delivered 25% Ibuprofen Gel in Chronic Periodontitis: A Randomized Controlled Clinical Trial. Journal of International Oral Health 2016; 8(6):651-656. [ Google Scholar]
  59. Batool F, Agossa K, Lizambard M, Petit C, Bugueno IM, Delcourt-Debruyne E, Benkirane-Jessel N, Tenenbaum H, Siepmann J, Siepmann F, Huck O. In-situ forming implants loaded with chlorhexidine and ibuprofen for periodontal treatment: Proof of concept study in vivo. Int J Pharm 2019 Oct 5; 569:118564. [ Google Scholar]
  60. Synthesis of a Novel Electrospun Polycaprolactone Scaffold Functionalized with Ibuprofen for Periodontal Regeneration: An In Vitro and In Vivo Study. Batool F, Morand DN,Thomas L, Bugueno IM, Aragon J, Irusta S,Keller L,Benkirane-Jessel, Tenenbaum H, Huck O. Materials (Basel). 2018 Apr 10; 11(4).
Submitted: 09 Nov 2019
Accepted: 28 Dec 2019
First published online: 02 Jan 2022
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