Locally Applied Slow-Release of Minocycline Microspheres in the Treatment of Peri-Implant Mucositis: An Experimental In Vivo Study

Background: The objective of this is preclinical investigation was to evaluate the differential drug sustainability and pharmacodynamic properties of two local minocycline microsphere carriers: chitosan-coated alginate (CA) and poly(meth)acrylate-glycerin (PG). Methods: Four dental implants were pla...

Full description

Bibliographic Details
Main Authors: Sung-Wook Yoon, Myong-Ji Kim, Kyeong-Won Paeng, Kyeong Ae Yu, Chong-Kil Lee, Young Woo Song, Jae-Kook Cha, Mariano Sanz, Ui-Won Jung
Format: Article
Language:English
Published: MDPI AG 2020-07-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/12/7/668
_version_ 1797562254971895808
author Sung-Wook Yoon
Myong-Ji Kim
Kyeong-Won Paeng
Kyeong Ae Yu
Chong-Kil Lee
Young Woo Song
Jae-Kook Cha
Mariano Sanz
Ui-Won Jung
author_facet Sung-Wook Yoon
Myong-Ji Kim
Kyeong-Won Paeng
Kyeong Ae Yu
Chong-Kil Lee
Young Woo Song
Jae-Kook Cha
Mariano Sanz
Ui-Won Jung
author_sort Sung-Wook Yoon
collection DOAJ
description Background: The objective of this is preclinical investigation was to evaluate the differential drug sustainability and pharmacodynamic properties of two local minocycline microsphere carriers: chitosan-coated alginate (CA) and poly(meth)acrylate-glycerin (PG). Methods: Four dental implants were placed unilaterally in the edentulous mandible of six beagle dogs. Each implant was randomly assigned to receive one of the following four treatments: (i) CA (CA-based minocycline), (ii) placebo (CA substrate without minocycline), (iii) PG (PG-based minocycline) and (iv) control (mechanical debridement only). After inducing peri-implant mucositis, the randomly assigned treatments were administered into the gingival sulcus twice at a 4-week interval using a plastic-tipped syringe. Drug sustainability and pharmacodynamic (clinical, radiographical and cell marker intensity) evaluations were performed after each administration. Results: The CA microspheres remained longer around the healing abutment compared to the PG microspheres at both administrations and a longer bacteriostatic effect was observed from CA (7.0 ± 5.7 days) compared to PG (1.2 ± 2.6 days). The efficacy of the applied therapies based on clinical, radiographical and histological analyses were comparable across all treatment groups. Conclusions: CA microspheres showed longer carrier and bacteriostatic effect sustainability when compared to PG microspheres, however, longer drug sustainability did not lead to improved treatment outcomes.
first_indexed 2024-03-10T18:26:33Z
format Article
id doaj.art-437e1c53cf8145088d978dcdeec0aaf0
institution Directory Open Access Journal
issn 1999-4923
language English
last_indexed 2024-03-10T18:26:33Z
publishDate 2020-07-01
publisher MDPI AG
record_format Article
series Pharmaceutics
spelling doaj.art-437e1c53cf8145088d978dcdeec0aaf02023-11-20T06:59:13ZengMDPI AGPharmaceutics1999-49232020-07-0112766810.3390/pharmaceutics12070668Locally Applied Slow-Release of Minocycline Microspheres in the Treatment of Peri-Implant Mucositis: An Experimental In Vivo StudySung-Wook Yoon0Myong-Ji Kim1Kyeong-Won Paeng2Kyeong Ae Yu3Chong-Kil Lee4Young Woo Song5Jae-Kook Cha6Mariano Sanz7Ui-Won Jung8Department of Periodontology, Research Institute for Periodontal Regeneration, Yonsei University College of Dentistry, Seoul 03772, KoreaDepartment of Periodontology, Research Institute for Periodontal Regeneration, Yonsei University College of Dentistry, Seoul 03772, KoreaDepartment of Periodontology, Research Institute for Periodontal Regeneration, Yonsei University College of Dentistry, Seoul 03772, KoreaCollege of Pharmacy, Chungbuk National University, Cheongju 28165, KoreaCollege of Pharmacy, Chungbuk National University, Cheongju 28165, KoreaDepartment of Periodontology, Research Institute for Periodontal Regeneration, Yonsei University College of Dentistry, Seoul 03772, KoreaDepartment of Periodontology, Research Institute for Periodontal Regeneration, Yonsei University College of Dentistry, Seoul 03772, KoreaSection of Graduate Periodontology, Faculty of Odontology, Complutense University of Madrid, 28040 Madrid, SpainDepartment of Periodontology, Research Institute for Periodontal Regeneration, Yonsei University College of Dentistry, Seoul 03772, KoreaBackground: The objective of this is preclinical investigation was to evaluate the differential drug sustainability and pharmacodynamic properties of two local minocycline microsphere carriers: chitosan-coated alginate (CA) and poly(meth)acrylate-glycerin (PG). Methods: Four dental implants were placed unilaterally in the edentulous mandible of six beagle dogs. Each implant was randomly assigned to receive one of the following four treatments: (i) CA (CA-based minocycline), (ii) placebo (CA substrate without minocycline), (iii) PG (PG-based minocycline) and (iv) control (mechanical debridement only). After inducing peri-implant mucositis, the randomly assigned treatments were administered into the gingival sulcus twice at a 4-week interval using a plastic-tipped syringe. Drug sustainability and pharmacodynamic (clinical, radiographical and cell marker intensity) evaluations were performed after each administration. Results: The CA microspheres remained longer around the healing abutment compared to the PG microspheres at both administrations and a longer bacteriostatic effect was observed from CA (7.0 ± 5.7 days) compared to PG (1.2 ± 2.6 days). The efficacy of the applied therapies based on clinical, radiographical and histological analyses were comparable across all treatment groups. Conclusions: CA microspheres showed longer carrier and bacteriostatic effect sustainability when compared to PG microspheres, however, longer drug sustainability did not lead to improved treatment outcomes.https://www.mdpi.com/1999-4923/12/7/668pharmacodynamicdrug sustainabilitychitosan-alginate microspheresperi-implant mucositislocal minocycline agent
spellingShingle Sung-Wook Yoon
Myong-Ji Kim
Kyeong-Won Paeng
Kyeong Ae Yu
Chong-Kil Lee
Young Woo Song
Jae-Kook Cha
Mariano Sanz
Ui-Won Jung
Locally Applied Slow-Release of Minocycline Microspheres in the Treatment of Peri-Implant Mucositis: An Experimental In Vivo Study
Pharmaceutics
pharmacodynamic
drug sustainability
chitosan-alginate microspheres
peri-implant mucositis
local minocycline agent
title Locally Applied Slow-Release of Minocycline Microspheres in the Treatment of Peri-Implant Mucositis: An Experimental In Vivo Study
title_full Locally Applied Slow-Release of Minocycline Microspheres in the Treatment of Peri-Implant Mucositis: An Experimental In Vivo Study
title_fullStr Locally Applied Slow-Release of Minocycline Microspheres in the Treatment of Peri-Implant Mucositis: An Experimental In Vivo Study
title_full_unstemmed Locally Applied Slow-Release of Minocycline Microspheres in the Treatment of Peri-Implant Mucositis: An Experimental In Vivo Study
title_short Locally Applied Slow-Release of Minocycline Microspheres in the Treatment of Peri-Implant Mucositis: An Experimental In Vivo Study
title_sort locally applied slow release of minocycline microspheres in the treatment of peri implant mucositis an experimental in vivo study
topic pharmacodynamic
drug sustainability
chitosan-alginate microspheres
peri-implant mucositis
local minocycline agent
url https://www.mdpi.com/1999-4923/12/7/668
work_keys_str_mv AT sungwookyoon locallyappliedslowreleaseofminocyclinemicrospheresinthetreatmentofperiimplantmucositisanexperimentalinvivostudy
AT myongjikim locallyappliedslowreleaseofminocyclinemicrospheresinthetreatmentofperiimplantmucositisanexperimentalinvivostudy
AT kyeongwonpaeng locallyappliedslowreleaseofminocyclinemicrospheresinthetreatmentofperiimplantmucositisanexperimentalinvivostudy
AT kyeongaeyu locallyappliedslowreleaseofminocyclinemicrospheresinthetreatmentofperiimplantmucositisanexperimentalinvivostudy
AT chongkillee locallyappliedslowreleaseofminocyclinemicrospheresinthetreatmentofperiimplantmucositisanexperimentalinvivostudy
AT youngwoosong locallyappliedslowreleaseofminocyclinemicrospheresinthetreatmentofperiimplantmucositisanexperimentalinvivostudy
AT jaekookcha locallyappliedslowreleaseofminocyclinemicrospheresinthetreatmentofperiimplantmucositisanexperimentalinvivostudy
AT marianosanz locallyappliedslowreleaseofminocyclinemicrospheresinthetreatmentofperiimplantmucositisanexperimentalinvivostudy
AT uiwonjung locallyappliedslowreleaseofminocyclinemicrospheresinthetreatmentofperiimplantmucositisanexperimentalinvivostudy