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Polymeric nanoparticles protect the resin-dentin bonded interface from cariogenic biofilm degradation

Toledano Osorio, Manuel,Osorio Ruiz, Raquel,Sánchez Aguilera, Fátima,Medina Castillo, Antonio Luis,Toledano Pérez, Manuel,Osorio Ruiz, María Estrella,Acosta, Sergio,Chen, Ruoqiong,Aparicio, Conrado

Abstract

The objective was to assess doxycycline (Dox) and zinc (Zn) doped nanoparticles' (NPs) potential to protect the resin-dentin interface from cariogenic biofilm. Three groups ofpolymeric NPs were tested: unloaded, loaded with zinc and with doxycycline. NPs were appliedafter dentin etching. The disks were exposed to a cariogenic biofilm challenge in a Drip-FlowReactor during 72 h and 7 d. Half of the specimens were not subjected to biofilm formation butstored 72 h and 7 d. LIVE/DEAD® viability assay, nano-dynamic mechanicalassessment, Raman spectroscopy and field emission electron microscopy (FESEM) analysiswere performed. The measured bacterial death rates, at 7 d were 46% for the control group, 51%for the undoped-NPs, 32% for Dox-NPs, and 87% for Zn-NPs; being total detected bacteriareduced five times in the Dox-NPs group. Zn-NPs treated samples reached, in general, thehighest complex modulus values at the resin-dentin interface over time. Regarding the mineralcontent, Zn-NPs-treated dentin interfaces showed the highest mineralization degree associatedto the phosphate peak and the relative mineral concentration. FESEM images after Zn-NPsapplication permitted to observe remineralization of the etched and non-resin infiltratedcollagen layer, and bacteria were scarcely encountered. The combined antibacterial andremineralizing effects, when Zn-NPs were applied, reduced biofilm formation. Dox-NPs exertedan antibacterial role but did not remineralize the bonded interface. Undoped-NPs did notimprove the properties of the interfaces. Application of Zn-doped NPs during the bondingprocedure is encouraged.

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Thismanusc ip hasbeenpublishedonlinein:Ac aBioma e ialiaMay2019 h ps://doi.o g/10.1016/j.ac bio.2020.05.002   1 Ti le: Polyme ic nanopa icles p o ec he esin-den in bonded in e ace om ca iogenic bio ilm deg ada ion. Running i le: Nanopa icles an ideg ada ion ac i i y a bonded den in. Au ho s: Manuel Toledano-Oso ioa, Raquel Oso ioa, Fá ima S Aguile aa, An onio Luis Medina-Cas illob, Manuel Toledanoa*, Es ella Oso ioa, Se gio Acos ac, Ruoqiong Chend, Con ado Apa icioe. Ins i u ion: a Uni e si y o G anada, Facul y o Den is y, Den al Ma e ials Sec ion. Colegio Máximo de Ca uja s/n 18071 – G anada - Spain. b c d Uni e si y o G anada, NanoMyP. Spin-O En e p ise. Edi icio BIC-G anada. A . Inno ación 1. 18016 - A milla, G anada, Spain. Bio o ge lab, CIBER-BBN, Edi icio LUCIA, Uni e si y o Valladolid, Paseo Belen 19, Valladolid 47011, Spain. Depa men o Diagnos ic and Biological Sciences, School o Den is y, Uni e si y o Minneso a, Minneapolis, MN, USA. e MDRCBB-Minneso a Den al Resea ch Cen e o Bioma e ials and Biomechanics, Depa men o Res o a i e Sciences, School o Den is y, Uni e si y o Minneso a, Minneapolis, MN, USA. *Co esponding au ho : P o . Manuel Toledano. Uni e si y o G anada, Facul y o Den is y Den al Ma e ials Sec ion Colegio Máximo de Ca uja s/n 18071 – G anada - Spain. Tel.: +34-958243788 Fax: +34-958240809 2 ABSTRACT The objec i e was o assess doxycycline (Dox) and zinc (Zn) doped nanopa icles' (NPs) po en ial o p o ec he esin-den in in e ace om ca iogenic bio ilm. Th ee g oups o polyme ic NPs we e es ed: unloaded, loaded wi h zinc and wi h doxycycline. NPs we e applied a e den in e ching. The disks we e exposed o a ca iogenic bio ilm challenge in a D ip-Flow Reac o du ing 72 h and 7 d. Hal o he specimens we e no subjec ed o bio ilm o ma ion bu s o ed 72 h and 7 d. LIVE/DEAD® iabili y assay, nano-dynamic mechanical assessmen , Raman spec oscopy and ield emission elec on mic oscopy (FESEM) analysis we e pe o med. The measu ed bac e ial dea h a es, a 7 d we e 46% o he con ol g oup, 51% o he undoped-NPs, 32% o Dox-NPs, and 87% o Zn-NPs; being o al de ec ed bac e ia educed i e imes in he Dox-NPs g oup. Zn-NPs ea ed samples eached, in gene al, he highes complex modulus alues a he esin-den in in e ace o e ime. Rega ding he mine al con en , Zn-NPs- ea ed den in in e aces showed he highes mine aliza ion deg ee associa ed o he phospha e peak and he ela i e mine al concen a ion. FESEM images a e Zn-NPs applica ion pe mi ed o obse e emine aliza ion o he e ched and non- esin in il a ed collagen laye , and bac e ia we e sca cely encoun e ed. The combined an ibac e ial and emine alizing e ec s, when Zn-NPs we e applied, educed bio ilm o ma ion. Dox-NPs exe ed an an ibac e ial ole bu did no emine alize he bonded in e ace. Undoped-NPs did no imp o e he p ope ies o he in e aces. Applica ion o Zn-doped NPs du ing he bonding p ocedu e is encou aged. Keywo ds: den in, deg ada ion, in e ace, nanopa icle, bio ilm 3 1. In oduc ion In den is y, es o a ions based on adhesi e esins a e widesp ead due o he aes he ic p ope ies and he handling cha ac e is ics o hese ma e ials. Bu adhesi e es o a ions ha e a high ailu e a e. A e 8 yea s, composi e es o a ions had a leas 50% g ea e ailu e pe cen age and 3.5 imes highe seconda y decay incidence han amalgam [1]. The adhesi e bond laye in eg i y o composi e es o a ion, i.e, he quali y o he in e ace be ween he oo h and he es o a ion, is he mos impo an ac o ha de e mines he long- e m success o es o a ions [1–4]. In clinical den is y, he mos equen ly in ol ed subs a e o adhesion is den in [5]. The s uc u e o den in is comp ised o a ound 50 ol% mine al. This mine al is p esen in he o m o apa i e c ys alli es, cha ac e ized by a ca bona e en ichmen and calcium de iciency. I is dis ibu ed be ween den inal ubules which un pa allel. The o he 50 ol% is wa e , collagen and o he mino non-collagenous p o eins [6]. Den in adhesion is p omo ed when he subs a e’s mine al phase is emo ed by acids and he oids o med by mine al a e filled wi h adhesi e esin, which is subjec ed o an in si u polyme iza ion, c ea ing he hyb id laye (HL) [7]. Collagen is no easily pene a ed by esins, a e acid e ching. Di e en ial den in di usion dep h be ween acids and esins p oduces a demine alized/non- esin in il a ed collagen laye , loca ed igh a he bo om, and named bo om o he hyb id laye (BHL). I is conside ed an in e acial mic ogap and he weak link a he composi e es o a ions [1]. The BHL is suscep ible o deg ada ion by in insic hos -de i ed ma ix me allop o einases (MMPs) o bac e ial ac i i y [8]. Bac e ial mic oleakage is he mos common complica ion among composi e es o a ions, and seconda y ca ies is he p incipal ailu e cause [2,3,9]. Bio ilm o ma ion a he es o a ion- oo h in e ace [10] is p obably assis ed by he gap o med be ween bo h s uc u es ha enables he coloniza ion o bac e ia [11], he eby acili a ing seconda y ca ies [3,12,13]. The pH dec ease caused by bac e ia acid p oduc ion, al e s he equilib ium and dissol es hyd oxylapa i e, leading o u he den in demine aliza ion [14–16]. Then, he exis ing gaps a he esin-den in bond in junc ion wi h an inc ease in le els o bac e ia a he pe ime e o 4 composi e ma e ials leads o a key ela ionship be ween mic obiology and adhesi e deg ada ion as c ucial elemen s in he ailu e o hese adhesi e es o a ions [1,17,18]. Bac e ia canno be elimina ed om he o al en i onmen , and hey ha e been shown o o m a mic o-ecosys em known as a bio ilm [1]. The educ ion o he pa hogenic impac o he bio ilm a he ma gin o he composi e es o a ion by enginee ing an i-ca iogenic ma e ials is desi ed [1,17–19]. Biocompa ible and non- eabso bable polyme ic nanopa icles (NPs), comp ised o me hac ylic acid, e hylene glycol dime hac yla e and 2-hyd oxye hyl me hac yla e co alen ly connec ed [20], has been p oposed o hinde he o ma ion o seconda y ca ies and ex end adhesi e es o a ions longe i y [21]. An ibac e ial and emine alizing agen s can be chemically a ached o he polyme ca ie h ough unc ional ca boxyl g oups ha a e along he su ace o he NPs [9,22]. Doxycycline and zinc ha e been p e iously doped on o hese NPs and an an ibac e ial [23] and an ibio ilm o ma ion e ec s we e demons a ed on hyd oxyapa i e discs [24]. Fu hemo e, NPs we e p e iously employed a he esin-den in bonded in e ace, and i was s a ed ha hey do no in e e e he bonding p ocess and also may p oduce collagen p o ec ion om den in MMPs [22,25]. The objec i e o his esea ch was o assess he doxycycline and zinc loaded-NPs po en ial o p o ec he esin den in in e ace om a ca iogenic bio ilm. Measu ing he e ec s o an ibac e ial agen s a he bonded in e ace in a simula ed o al en i onmen is challenging. A mul i ac o ial dele e ious e ec o bac e ia a he bonded in e ace has been epo ed [26]. A LIVE/DEAD® s aining echnique con ibu es o de e mine he p esence and g ow h o he bio ilm a he esin-den in in e ace [17]. Bac e ial localiza ion may also be quali a i ely analyzed by scanning elec on mic oscopy. Nano-DMA ep esen s a c ucial ool o de ec he bonded in e ace deg ada ion ough educ ion in mechanical p ope ies o he bonded in e ace ha p ima y esul ed om den in demine aliza ion [27]. High biochemical speci ici y analysis o he esin-den in in e ace h ough complemen a y Raman spec oscopy has also been p oposed [28]. The null hypo hesis o be es ed is ha in il a ion o doxycycline and zinc loaded-NPs in o e ched den in, p e ious o he esin applica ion s ep, does no exe p o ec ion o he hyb id 5 laye om he in i o deg ada ion ac i i y o a ca iogenic bio ilm. 2. Ma e ials and me hods 2.1. Nanopa icles ab ica ion and loading PolymP-n Ac i e nanopa icles we e used (NanoMyP®, G anada, Spain). These pa icles a e syn he ized ollowing a polyme iza ion p ecipi a ion p ocedu e. NPs a e composed by a main monome , 2-hyd oxye hyl me hac yla e, a c oss-linke , e hylene glycol dime hac yla e, and a unc ional monome , me hac ylic acid. De ailed desc ip ion o NPs composi ion and p oduc ion is a ailable [20]. NPs zinc-doping is ob ained ia imme sion o 25 mg o NPs in 25 ml aqueous solu ions o ZnCl2 (40 mgL-1), o in 25 ml o doxycycline hycla e aqueous solu ion (Sigma Ald ich, ChemieGmbh, Rieds , Ge many) a 750 mgL-1, du ing 30 min unde cons an shaking o 20 and 90 min espec i ely. Suspensions we e hen subjec ed o a cen i uga ion p ocess o 20 min (7,800 pm/G- o ce=6,461) and he pa icles washed in phospha e bu e ed solu ion (PBS) and de ached om he supe na an [25,29]. The a ained abso p ion equilib ium o zinc as a ime unc ion and ZnCl2 solu ion concen a ions was p e iously assessed [30] and he maximum a ained zinc complexa ion alue (2 µg Zn/mg NPs) was used o load NPs in he p esen s udy. Doxycycline doping alues o NPs as a unc ion o incuba ion ime and doxycycline concen a ions was also measu ed [30] and he maximum doxycycline adso p ion alue o 27.1 µg Dox/mg NPs was selec ed o load NPs o he p esen esea ch. I has been p e iously shown ha he size o NPs does no change a e loading, and no agglome a ion is p oduced. Hyd odynamic size dis ibu ion o nanopa icles is NPs 250.1 ± 7.5 nm, Dox-NPs 244.4 ± 9.8 nm and Zn-NPs 225.9 ± 8.9 nm [31]. 2.2. Mul ispecies bio ilm s ocks F ozen (-80ºC) mul ispecies bio ilm s ocks om mul iple subjec s we e used. Plaque was collec ed om den al es o a ions ma gins [32]. Uni e si y o Minneso a Ins i u ional Re iew Boa d app o ed he o iginal human plaque sampling p o ocol used o p epa e he s ocks. Employed s ocks om mic ocosm bio ilms we e ep esen a i e o he o al mic obio a. Bio ilm alida ion and a comple e bio ilm cha ac e iza ion may be ound in Rudney e al., [33]. 6 2.3. Den in disks p epa a ion The den in disks p epa a ion was made ollowing Li e al., 2014 [18]. Disk specimens we e made using bo ine inciso s. The bo ine ee h we e s o ed in 1.0% Chlo amine T solu ion. The media was eplaced once a week by eshly p epa ed solu ions and s o ed in 4◦C be o e use. The c owns we e cu o a he cemen -enamel junc ion (CEJ) wi h a low-speed diamond saw (Isome , Buehle , LakeBlu , IL, USA) unde cooling wa e o p o ide he oo den in po ion. These specimens we e hen immed down in o den in cylinde s o 5 mm in diame e (concen ic and pa allel wi h he enla ged oo canals), and he oo canals we e enla ged o 2 mm in diame e using Ga es–Glidden d ills. The cylinde s we e ans e sely cu o p oduce ound disks o abou 4 mm. A e his p ocess, hey we e insed 3 imes wi h dis illed wa e , s o ed in 1.0% Chlo amine T solu ion o 7 days a 4◦C be o e being used. A o al o 88 disks we e p epa ed. 2.4. Den in-composi e disks ab ica ion The disks we e hen insed in dis illed wa e and d ied ou . To p oceed wi h he composi e illing, a common adhesion p o ocol was ollowed. The inne su ace o he disks was subjec ed o an e ching p ocess wi h 35% phospho ic acid du ing 20 s. The disks we e subsequen ly insed wi h dis illed wa e and sligh ly d y. Disks we e andomly di ided in o ou g oups (n=22), ega ding NPs applica ion: 1) NPs we e no applied (e hanol was used ins ead o he NPs suspension); 2) undoped NPs; 3) Dox-NPs; and 4) Zn-NPs. The di e en NPs in e hanol suspensions (10 mg/ml) we e hen applied on he e ched su aces o he disks be o e he adhesi e applica ion. Single Bond (SB) (3 M ESPE, S . Paul, MN, USA) adhesi e, was placed o he inne su ace and polyme ized, ollowing manu ac u e ’s ins uc ions. The disks we e comple ely illed wi h Z-100TM (3 M ESPE, S . Paul, MN, USA), which was applied inc emen ally and ligh cu ed o 40 s. The wo su aces o he disks we e hen g ound la (180-g i ) (Figu e 1). 2.5. In i o bio ilm challenging model Six een samples om each g oup we e andomly selec ed (n=64). Be o e being exposed o bio ilm, he bo om and he side su aces o disks we e co e ed wi h acid esis an nail 7 a nish. F om he uppe su ace, only he ou e pa o he disk was nail a nished (lea ing unp o ec ed he esin-den in in e ace and he esin su ace). Samples we e imme sed o 5 min in 75% e hanol, ai -d ied and s e ilized unde UV ligh o 20 minu es [32]. The ollowing s eps we e pe o med inside he high e iciency pa icula e ai (HEPA) enclosu e. The unp o ec ed (no co e ed wi h nail a nish) esin-den in in e ace and esin su aces we e coa ed wi h 10µl il e s e ilized whole sali a o 5 minu es. 10µl o mul ispecies bio ilm solu ion (769NS) om a 1:100 dilu ion o he bac e ial s ock we e inocula ed on he op o he sali a coa ing o ano he 5 minu es. Disks whe e hen placed in a well pla e (one disk pe well) and co e ed wi h 1.5 ml o s e ile basal mucin medium (BMM) and incuba ed a 37°C, 5% CO2 o 24 h. A e his pe iod, he samples we e ans e ed in o a 4 channel D ip-Flow Reac o wi h a 37ºC incuba o wi h a pump a e o 0.28 ml/minu e. Two ime poin s we e es ablished o analyzing he bio ilm samples: 72 h (24 h o pla e + 48 h o eac o ) and 1 week (24 h o pla e + 6 d o eac o ). Hal o he samples (n=32) we e subjec ed o each ime poin . The o he wen y- ou samples, 3 om each g oup we e incuba ed ollowing he same p ocedu e bu wi hou bac e ia inocula ion. A e ge ing hem ou o he eac o di e en ea men s we e ca ied ou depending on he analyzing me hod. 2.6. LIVE/DEAD® iabili y assay Th ee disks pe each g oup, om hose subjec ed o bac e ia challenge, we e gen ly subme ged in o 0.9% NaCl o emo e he una ached bac e ia. Fo cell iabili y assessmen , he luo escen s ains solu ion was p epa ed (L7012, LIVE/DEAD® BacLigh Bac e ial Viabili y Ki , The moFishe Scien i ic, Wal ham, MA, USA) by adding 3 µl o SYTO9 g een s ain and 3 µl o P opidium iodide ed s ain o 1 ml o s e ilized Milli-Q ul apu e wa e . 100 µl o s aining solu ion was added. A e 20-30 min in ligh -p o ec ed incuba ion a oom empe a u e, he bio ilms g own on op he unp o ec ed a eas o he disks we e analyzed by con ocal lase scanning mic oscopy (CLSM) wi h a mul ipho on con ocal mic oscope (A1R-HD, Nikon Ins umen s Inc., Japan). A 25x wa e imme sion objec i e (Apo LWD, 1.1 NA) was used o di ec ly isualize he bio ilms. Fluo escence emissions we e collec ed a 488 nm o Sy o9 (li ing cells) and a 561 nm o p opidium iodide (dead cells). 512 x 512 and 1024 x 1024 pixel 8 a eas we e scanned, and he Z-s acks we e eco ded e e y 0.375 µm. Images we e analyzed using an image analysis so wa e (ImageJ B, Na ional Ins i u es o Heal h, Be hesda, Ma yland, USA), by measu ing oxel in ensi ies om wo-channel images, and he e o e calcula ing he cell iabili y pe cen age wi hin he s acks. Subs ac ion o he backg ound signal was pe o med. 2.7. Nanodynamic mechanical (NanoDMA) assessmen Th ee di e en disks om each g oup we e subjec ed o nanoDMA. Disks we e sligh ly polished (2400 o 4000 g i and 1 µm diamond pas e) and ho oughly washed wi h deionized wa e . P ope y mappings we e ealized using a Ti-750D T iboInden e (Hysi on, Inc., Minneapolis, MN) equipped wi h nano-DMA III, a comme cial nano-DMA package. The nanoinden e ip was calib a ed agains a used qua z sample using a quasis a ic o ce se poin o 5 µN o main ain con ac be ween he ip and he sample su ace. A dynamic (oscilla o y) o ce o 5 µN was supe imposed on he quasis a ic signal a a equency o 200 Hz. Based on a calib a ion modulus o he ip alue o 1.1400E+3 N/mm2 o he used qua z, he bes - i sphe ical adius app oxima ion o ip was ound o be 150 nm, o he selec ed nano-DMA scanning pa ame e s. Modulus mapping o ou samples was conduc ed by imposing a quasis a ic o ce se poin , Fq =5 µN, o which we supe imposed a sinusoidal o ce o ampli ude FA=1.8 µN and equency =200 Hz. Da a om egions app oxima ely 20×20 µm in size we e collec ed using a scan a e o 0.2 Hz. Each scan esul ed in a 256×256 pixel da a a ay. Specimens we e scanned in he hyd a ed condi ion. Regions o in e es o analysis we e selec ed jus below he adhesi e laye . Unde s eady condi ions (applica ion o a quasis a ic o ce) he inden a ion modulus o he es ed sample, E, was ob ained by applica ion o di e en models ha ela e he inden a ion o ce, F, and dep h, D [34]. Da a om he hyb id laye (HL), bo om o hyb id laye (BHL) we e acqui ed, as ep esen ed in he Fig. 1. 2.8. Raman spec oscopy The same den in su aces men ioned abo e we e subsequen ly s udied by Raman spec oscopy. Fo his analysis, a dispe si e Raman spec ome e /mic oscope (Ho iba Scien i ic Xplo a, Villeneu e d´Ascq, F ance) wi h a 785-nm diode lase h ough a X100/0.90 NA ai 15 educed om 24 h o 7 d o one hi d, howe e i should also be no ed ha he o al bac e ial coun s a he bonded in e ace was educed abou i e imes. I is hypo hesized ha su i ing bac e ia a e 7 d, we e ewe in numbe , bu mos esis an o doxycycline e ec . A he con a y in he case o Zn-NPs he o al bac e ial coun s was simila a e 24 h and 7 d, bu he an ibac e ial ac i i y (dead o inju ed cells) was almos wo- old a e 7 d han a 24 h ime- poin , showing a slowe an ibac e ial ac i i y o Zn-NPs. I has been p e iously epo ed [41] ha LIVE/DEAD® dyes may no be used as an exac quan i a i e measu emen o cell dea h. P opidium iodide s ained cells ( ed cells) may be alsely iden i ied as dead cells, and ep esen cells ha a e inju ed, dead o s a ing iable cells. The e o e ed cells pe cen ages should be aken wi h cau ion. When analyzing FESEM images o hose g oups (Zn-NPs and Dox-NPs a e 7 d), i is clea ha bac e ia we e no easily obse ed a any o he bonded in e aces (Figs. 4b, 4d, 4g, 4h), co obo a ing LIVE/DEAD esul s. In he es o he g oups, bio ilm s uc u es ancho ed and de eloped adhe ence and pene a ion h ough he BHL in den in specimens incuba ed no only a 72 h, bu also a e 7 d (Figs. 3bSI, 3dSI). Den in emine aliza ion a he hyb id laye was encoun e ed when Z-NPs we e applied (Figs. 4g,4h). Howe e , an ad anced den in demine aliza ion was also obse ed a FESEM images o in e aces ea ed wi h Dox- NPs (Figs. 4b, 4d). T ough Raman analysis i was demons a ed ha all g oups e lec ed demine aliza ion a he esin-den in in e ace (Table 2), as he symme ic bending mode ( 2) o phospha e (PO43-) a 431 cm-1 was g ea e han a 446 cm-1 peaks [37] in all cases. I should be conside ed ha NPs a e no e ained by physical abso p ion, bu o ming p ima y bonds wi h demine alized collagen. Dislodging du ing he den in bonding will no occu as pa icle binding o demine alized collagen is p oduced. I may be explained by (1) he esul o he high a ini y be ween he nega i ely cha ged polyme ic NPs (−43.3 mV) and he posi i ely cha ged demine alized den in collagen and (2) due o he binding o COO− g oups om NPs o NH+ si es a den in collagen. Then, pa icle e en ion a he demine alized den in su ace is p oduced, and i is impo an as NPs collagen binding is necessa y o exe a emine aliza ion e ec [25,45]. I is also impo an o s ess ha es ed NPs loca ed a he esin- den in bonded in e ace do no p oduce speci ic spec al ea u es o luo escence ha may 16 o e lap o obscu e Raman signals, as p e iously demons a ed ough a de ailed Raman analysis o he di e en subs a es (polyme s and den in) a hese bonded in e aces demons a ed [45]. E en when he comple e Raman spec a we e p o ided, jus he ele an spec al ea u es we e assigned and commen ed in he p esen manusc ip , some mo e in o ma ion abou Raman analysis o den in bonded in e ace ea ed wi h he p esen expe imen al NPs is p esen ed somewhe e else [45]. Bo h he s o age modulus (E') and he loss modulus (E'') a e in ol ed in he iscoelas ic exp ession o he complex modulus (E*), only E* will be discussed. The complex modulus is a measu e o he ma e ial esis ance o dynamic de o ma ion [46]. The demine alized BHL is he Achilles’s heel o adhesion o den in, p obably, which mos likely de e mine he low es o a ion longe i y [1]. A 7 d o s o age, he BHL o specimens ea ed wi h Zn-NPs and exposed o bio ilm challenge showed he highes E* (Fig. 2), deno ing ad anced in a ib illa emine aliza ion [47]. Complex modulus ou comes show ha he g een and/o yellow egions obse ed a he bo om o he hyb id laye , when Zn-NPs we e applied and analyzed a e 7 d (Fig. 2aSI), had highe alues han he es o he specimens, sugges ing he occu ence o minimal i any demine aliza ion, and hus den in emine aliza ion [21] (Fig. 2). In gene al, complex modulus alues o den in ea ed wi h Zn-NPs we e be ween wo and ou imes old hose o con ol g oup, and i is consis en wi h o he s udies [31,45]. Zinc has been p e iously shown o p oduce calcium/phospha e p ecipi a ion and den in emine aliza ion wi h a high inc ease in mechanical p ope ies [48]. I has also been shown when his new mine al is o med in he p esence o zinc, an exchange be ween Zn2+ and Ca2+ occu s in i o, o ming a subs i u ed apa i e compound h ough an isomo phous subs i u ion [49]. A highe nanoha dness and lowe solubili y was ound in his zinc-subs i u ed mine alized laye [49,50]. Den in ea ed wi h Zn-NPs a e 7 d p esen s Raman bands a 579, 590, cm-1 ( 4 asymme ic bending mode PO43-) e lec ed he lowes peak alues among g oups (Table 2), e oking he in si u p esence o sound den in [37]. The lowes in ensi y a io plo showed a 579/ 959, 590/ 959 (Table 2), also demons a ed den in emine aliza ion a he in e ace [37,51]. This mine al p ecipi a ion p omo ed ac i e den in emodeling wi h inc eased ma u i y which was 17 sus ained on a high collagen quali y pa ame e (1.37) ( a io 1674 cm-1/1690 cm-1) [40] (Table 2) and highe mechanical p ope ies [31,45]. These new mine al o ma ions, absen in he es o he g oups, we e obse ed as mul iple od-like igu es ha illed he in a ubula den in lumen a bo h pe i ubula and in e ubula den in [45] (Fig. 4h). To p e en s ess concen a ion zones and o a oid c ack p opaga ion ac oss he su ace, he emine alized den in should abso b mechanical shock wa es. E* esul s e ealed ha he e is homogenei y in he mechanical p ope ies dis ibu ion be ween HL and BHL, when samples we e ea ed wi h bo h Dox-NPs and Zn-NPs (Fig. 2). HL in bo h g oups showed highe E* han he BHL (1.28 and 1.03 old, espec i ely) enabling, he eby, he ene gy dissipa ion ac oss hei s uc u es. Thus, a 7 d o s o age, nano-DMA e ealed ha he e is he e ogenei y in he mechanical p ope ies dis ibu ion a bo h HL and BHL in he g oup o samples ea ed wi h Dox-NPs, exposed o bio ilm challenge, making he issue p one o c acking [52,53]. This b eakdown o den in, p e e en ially occu ed a he HL [54], p ecisely whe e bands a 579, 590, cm-1 showed he highes peak alues (41.68 and 38.75, espec i ely), which sugges s he g ea es demine aliza ion zone [37] among all g oups (Table 2). The ailu e coincided wi h he o med gap in he esin-den in in e ace which clea ly caused he HL o be de ached om he BHL (Fig. 4e). The p esence o hese c acks suppo s he assump ion ha he c acks can acili a e acids pene a ion. Howe e , seconda y ca ies o ma ion may be impai ed [55], due o bo h he inhibi o y e ec o MMPs by doxycycline [56] and he an ibac e ial p ope ies o Dox- NPs [23,24]. Dox-NPs applica ion did no induce mine als p ecipi a ion o den in emine aliza ion (Fig. 3) [31]. Howe e , he ein o ced den in mic os uc u e and he ela i ely imp o ed mechanical p ope ies (Fig. 2) a e p obably due o he high collagen-c osslinking ha was ob ained a e Dox-NPs applica ion [45,57,58] (Table 2). The main componen o AGE (ad ance glyca ion end p oduc s) is he pen osidine [40]. Pen osidine Raman signal a ained he highes alues in Zn-NPs- ea ed samples (14.38) (Table 2) when compa ed wi h he es o g oups, indica ing ad anced sca olding o collagen and g ea e po en ial o u he emine aliza ion [40]. E en a 72 h o s o age, Dox-NPs- ea ed den in a ained he lowes 18 s o age modulus (Fig. 2 SI) (Table 1SI) wi h minimal emine aliza ion (Figs. 3SIe, 3SI ). Raman peaks de ec ed a 1400cm-1 co espond o bonds o Ca-COO and can be associa ed wi h Ca-Dox complexes ha a ec he p ima y nuclea ion, in e e ing wi h mine al p ecipi a ion and inhibi ing mine aliza ion [59]. Ca-COO peaks became highe o e ime (Fig. 3 ), and his abili y o chela e calcium ions, may be esponsible o some de e io a ion o he mechanical p ope ies [59] (Fig. 2). The ini ial bu s o Doxycycline elease om NPs, which has been p e iously desc ibed [23] was con i med by he hie a chical clus e analysis (HCA) o he Raman spec a a e 72 h (Fig. 3c). The h ee plo s co esponded o he di e en HCA a iances ha appea ed below 750 cm-1 Raman shi s. They s ill appea ed bu became lowe a e 7 d (Fig. 3d), p obably indica ing mino d ug elease om he deli e y sys em a e his ime (NPs) [23,59]. A 7 d o s o age, Dox p esence inc eased a he esin-den in in e ace and so he Dox-Ca complexes (Fig. 3 ). This ou come wa an ed he an ibac e ial p ope ies [24] o Dox-NPs o e ime. The lowe nano-DMA ou comes when bo h con ol o undoped-NPs g oups we e exposed o bio ilm challenge 7 d co ela ed wi h e ealed a eas o demine aliza ion (Figs. 4b, 4d, espec i ely) as a p oduc o incomple e esin imp egna ion o demine alized den in. E en a 72 h o s o age, undoped-NPs ea ed den in showed he lowes loss modulus, among g oups a bo h he HL (2.61 GPa) and he BHL (2.51 GPa) (Table 1SI) (Fig. 2gSI). This also co ela ed wi h he high RMC alues (Table 2) ha we e ob ained a e applying unloaded-NPs. RMC exp esses he ela i e p esence o mine als [phospha e, (PO43-)] e e ed o p o eins (phenyl g oup), [60]. The Raman peak o phenyl in den in ea ed wi h undoped-NPs showed he low in ensi y ha was ob ained in he p esen s udy (43.06) among he g oups in which NPs we e applied (Table 2). This ac e lec ed he p esence o sca ce ma ix con en and damaged collagen (Figs. 4c, 4d), which indi ec ly aised he quo ien RMC (Table 2) [57]. The lack o esin in il a ion and p ope den in emine aliza ion in specimens ea ed wi h undoped-NPs allow he bac e ia o ha e access o colonize he demine alized den in collagen, along he in e ace [61] (Figs. 4b, 4d). As a esul , bac e ia could pene a e h ough he demine alized po es, oids, c acks and open ubules [31] allowing he p esence o ma u e bio ilm wi hin he s uc u es o he esin-den in in e ace, e en a 72 h o s o age (Figs 4b, 4d, 3bSI, 3dSI). 19 Acco dingly, i is specula ed ha bac e ia and he exis ence o demine alized den in a he BHL, may syne gis ically p omo e seconda y oo h ca ies o ma ion. The bonded in e ace is hen deg aded by o al bac e ia leakage a he gaps o he BHL. Bac e ia can di ec ly colonize and bind o demine alized collagen p esen in den in [2], o ming a bio ilm and in ec ing he den inal issues [17]. Bac e ia, h ough adhesins p esen a he cell memb ane and in junc ion wi h o he collagen-binding p o ein and se ine p o eases, ancho age and colonize he non- esin co e ed o unp o ec ed collagen, whe e hey exe hei p o eoly ic and demine alizing ac ion [32,62], p omo ing in e acial deg ada ion. Zinc and doxycycline a e an ibac e ial [63] and also po en ma ix me allop o einases (MMPs) inhibi o s; he eby, hey a e collagen p o ec o s [56]. This poin has gained clinical ele ance a e s udies pe o med by Fine , as i was demons a ed ha den inal pa hogenic bac e ia p oduce MMPs ha may deg ade collagen acili a ing den in in asion [64]. Consis en wi h hese esul s i was also shown ha a MMPs inhibi o wi h no an ibac e ial ac i i y was able o enhance ma ginal in eg i y and o educe in e acial bac e ial ing ess and bac e ial biomass in den in- esin bonded in e aces [65]. The mine al p ecipi a ion in specimens ea ed wi h Zn-NPs (Fig. 4h) lead o a educed bac e ial pene a ion, when compa ed wi h hose ea ed wi h Dox-NPs (Fig. 4 ), a e 7 d o bio ilm challenge. The e o e, he emine alizing and an ibac e ial e ec s we e combined when Zn-NPs we e applied. In his manusc ip , we ha e a ained a posi i e ou come in one o he highes no ewo hy a eas o conce n in adhesi e den is y, he s abili y o he den in bonding in e ace. This wo k p o ides a amewo k o u he esea ch ying o de elop u u e ma e ials wi h in insic an imic obial e ec s, and ma e ials which will no only unc ionally es o e den in bu also s imula e biological esponses ha inc ease emine aliza ion and na u al den in epai [66]. The p esen s udy used a mul ispecies bio ilm om a s ock o plaque mic ocosm bio ilm. This complex and clinically ele an bio ilm p o ides expe imen al condi ions ha can be used o assess he po en ial clinical e icacy o he expe imen al NPs [41]. Howe e , i is impo an o no e ha he an imic obial NPs do no selec i ely kill ce ain pa hogens. They ac 20 as b oad spec um an imic obials. As such, hey indisc imina ely will a ec commensal bac e ia, which can comp omise he balance o species in he heal hy o al bio ilm. Fu he esea ch abou po en ial e ec s on bio ilm dysbiosis should be pe o med. The p esen esea ch is new no only ega ding he use o hese unique loaded NPs bu also, because o he mul iple complemen a y esea ch es ing and cha ac e iza ion echniques and ools pe o med o e alua e he e ec o he bac e ial challenge, a he bonded esin-den in in e ace. Nanomechanical, mo phological and chemical conside a ions we e inno a i ely aken oge he o analyze he da a and d aw conclusions. The esul s o his esea ch a e clinically ele an . Bu his s udy also has some limi a ions: 1) an ibio ics may p oduce bac e ial esis ance and dysbiosis which a e cu en global conce ns; he e o e, u he esea ch is needed o asce ain he long- e m e ec o es ed NPS a he bonded in e ace, 2) he employed d ip low eac o does no ake in o conside a ion he e ec o mechanical loading in gap o ma ion, bac e ial pene a ion and he consequen demine aliza ion, i dese es u u e esea ch, 3) he use o bo ine adicula den in, 3) he pe pendicula di ec ion o he den inal ubules espec o he bonded in e ace which a ies om he o ien a ion ound in eal clinical condi ions and 4) c ea ing ca i ies wi h a high C ac o , a o ing gaps o ma ion and bac e ial coloniza ion. This implies ha cau ion mus be implemen ed when ying o ex apola e he cu en ou comes o clinical condi ions. Fu u e clinical s udies ocusing on he esin-den in in e ace deg ada ion a e encou aged. 5. Conclusions The combined an ibac e ial and emine alizing e ec s o Zn-NPs a he den in in e ace dec eased he hyb id laye deg ada ion media ed by he es ed in i o ca iogenic bio ilm. The e was a signi ican bac e ial iabili y educ ion, o e ime, when Dox-NPs we e applied. Applica ion o Dox-NPs on den in also p oduced ad anced sca olding o collagen bu did no acili a e esin-den in in e ace emine aliza ion. 21 Disclosu e The au ho s epo no con lic s o in e es in his wo k. Acknowledgemen s This wo k was suppo ed by he Minis y o Economy and Compe i i eness and Eu opean Regional De elopmen Fund [MAT2017-85999P MINECO/AEI/FEDER/UE] and Uni e si y o G anada Resea ch & T ans e P og am. The au ho s acknowledge P o esso Joel D. Rudney, Uni e si y o Minneso a o acili a ing he use o mic obiology acili ies and access o he plaque samples. Mul ipho on con ocal lase mic oscope was pe o med a he Uni e si y o Minneso a Imaging Cen e s (h p://uic.umn.edu). Re e ences [1] P. Spence , Q. Ye, J. Pa k, E.M. 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Clegho n, Ex i o de ec ion and cha ac e iza ion o ea ly den al ca ies by op ical cohe ence omog aphy and Raman spec oscopy, J. Biomed. Op . 10 (2005) 031118. 31 Figu e 1. Figu e 1. Schema ic illus a ion p esen ing disks p epa a ion mode and he obse a ion zone o all expe imen al p ocedu es ( he esin-den in bonded in e ace). Regions o in e es o analysis we e selec ed jus below he adhesi e laye . HL: Hyb id Laye ; BHL: Bo om o Hyb id Laye ; PD: Pe i ubula Den in; ID: In e ubula Den in; : esin ag; T: den inal ubule. 32 Figu e 2. Figu e 2. (a,b) Complex Modulus (GPa) a he di e en esin-den in bonded in e aces, measu ed a bo h hyb id laye (HL) (a) and bo om o hyb id laye (BHL) (b) loca ions espec i ely. HL and BHL we e analyzed independen ly. Simila capi al le e s indica e no signi ican di e ences be ween bio ilm g oups wi hin he same NPs g oup and ime-poin s (p<0.01). Compa isons wi hin he same bio ilm and NPs g oups a e indica ed wi h simila lowe case le e s, indica ing no signi ican di e ences be ween ime-poin s (72 h and 7 d o s o age) (p<0.01). Numbe s indica e signi ican di e ences among NPs g oups, wi hin he same bio ilm and ime-poin s g oups (p<0.05). 33 Figu e 3. Figu e 3. 2D mic o-Raman map (20 x 20 µm) o he phospha e peak (961 cm-1) in ensi ies a he esin-den in in e ace ob ained a e Dox-NPs (a) and Zn-NPs (b) applica ion, a 7 d o s o age wi h bio ilm challenge. Raman spec a om hie a chical clus e analysis (HCA) esul s o samples ea ed wi h Dox-NPs, a 72 h (c), 7 d (d) o s o age wi h bio ilm challenge. Th ee le els o HCA clus e ing a e shown. Va iances o dis inc colo s ha e di e ences in Raman spec al dis ibu ion and chemical composi ion. Each pe cen age clus e is assigned o a di e en colo ( ed, g een and blue). Raman spec a om hie a chical clus e analysis (HCA) esul s a he hyb id laye o samples ea ed wi h Zn-NPs, a 72 h and 7 d o s o age wi h bio ilm challenge (e). A unca ed segmen (1200-1500 Raman shi s, cm-1) o mic o-Raman analysis ( ) co esponding o he double peak o doxycycline (1252 cm-1, 1270 cm-1) and calcium-doxycycline complexes (1400 cm-1) a bo h 72 h and 7 d s o age ime in bio ilm challenge, may be obse ed. 34 Figu e 4. 35 Figu e 4. Field emission scanning elec on mic oscopy images o he esin-den in in e - di usion zone es ed a e 7 d o s o age. a, b: Den in in e ace bonded wi h Single Bond adhesi e and wa e /e hanol as p e- ea men . Open (a ows) and illed (poin e s) den inal ubules we e obse ed c ossing o e he den in su ace. Demine alized collagen ibe s (as e isks) below he hyb id laye (HL) and mul iple bac e ia (double a ows) we e disco e ed in a. A a highe magni ica ion (b), non-mine alized and esin unp o ec ed collagen ibbe s (a ows) we e appa en . Collagen ibbe s showed educed diame e . Bac e ial ancho age on unp o ec ed collagen was e iden in b (poin e s) [Scale ba : 3 µm (a), 1 µm (b)]. c, d: Den in in e ace in which undoped-NPs we e in il a ed be o e bonding. Mine al deposi s (double a ows), denuded collagen ibe s (a ows) and adhesi e esin (as e isks) we e shown. Collagen ibbe s exhibi ed diame e s o abou 100 nm, and pe iodical s ia ions ( iangles). A p o use bac e ial conso ium colonized he in il a ed den in (poin e s), in c. Dis up ed collagen ibbe s showing loose ends which a e non mine alized o esin p o ec ed we e e iden in d (a ows). Solely ew indi idual (poin e s) o associa ed ( aced a ows) NPs appea ed on o he deg aded den in su ace. Localized mine aliza ion was e iden (double a ows) [Scale ba : 1 µm (c), 100 nm (d)]. e, : Den in in e ace whe e Dox-NPs we e in il a ed be o e bonding. A e icula pa e n o s agge ed and demine alized collagen ib ils (a ows) was obse ed below he HL, c ossing o e he in e ubula den in a he BHL. Wi hin he esin-den in in e ace, a gap de aching he HL om he BHL was o med (double a ows). Minimal amoun o bac e ia was ad e ed (poin e s) on o he non emine alized den in, in e. A high magni ica ion, s agge ed and demine alized collagen ib ils (a ows) we e obse ed co e ing wo neighbo demine alized and non esin-in il a ed ubules, which appea ed o ally emp y, in . A pe i ubula den in, mine al o med a colla a ound each ubule lumen obse ed (as e isks). Mine alized collagen ibe s and NPs o med he ubula wall (poin e s) [Scale ba : 1 µm (e), 300 nm ( )]. g, h: Den in in e ace whe e Zn-NPs we e in il a ed be o e bonding. The esin composi e (RC) and he adhesi e (ADH) we e isible. Thick HL was obse ed and mine alized collagen ib ils we e no no iceable below new mine al deposi s. Tubules we e sca cely obse ed (a ows). Mine aliza ion was de ec ed as a dense ne wo k o mul ilaye ed mine al deposi s on he den in su ace (as e isks) and bac e ial we e ha dly encoun e ed, in g. In e ubula (ID) and pe i ubula den in (PD) appea ed en i ely emine alized. Tubules we e almos o ally occluded (poin e s). A comple e emine alized web o collagen ibbe s (double a ows) we e disco e ed a he bo om o he hyb id laye (BHL) in h. Fib ils exhibi ed a wid h o a ound 100-200 nm and he ypical 67-nm pe iodici y ( iangles). Minimal amoun o bac e ial colonized he specimens. [Scale ba : 3 µm (g), 300 nm (h), 100 nm (inse )]. 36 Supplemen a y Ma e ial Ti le: Polyme ic nanopa icles p o ec he esin-den in bonded in e ace om ca iogenic bio ilm deg ada ion. Running i le: Nanopa icles an ideg ada ion ac i i y a bonded den in. Au ho s: Manuel Toledano-Oso ioa, Raquel Oso ioa, Fá ima S Aguile aa, An onio Luis Medina- Cas illob, Manuel Toledanoa*, Es ella Oso ioa, Se gio Acos ac, Ruoqiong Chend, Con ado Apa icioe. Ins i u ion: a Uni e si y o G anada, Facul y o Den is y, Den al Ma e ials Sec ion. Colegio Máximo de Ca uja s/n 18071 – G anada - Spain. b c d Uni e si y o G anada, NanoMyP. Spin-O En e p ise. Edi icio BIC-G anada. A . Inno ación 1. 18016 - A milla, G anada, Spain. Bio o ge lab, CIBER-BBN, Edi icio LUCIA, Uni e si y o Valladolid, Paseo Belen 19, Valladolid 47011, Spain. Depa men o Diagnos ic and Biological Sciences, School o Den is y, Uni e si y o Minneso a, Minneapolis, MN, USA. e MDRCBB-Minneso a Den al Resea ch Cen e o Bioma e ials and Biomechanics, Depa men o Res o a i e Sciences, School o Den is y, Uni e si y o Minneso a, Minneapolis, MN, USA. *Co esponding au ho : P o . Manuel Toledano. Uni e si y o G anada, Facul y o Den is y Den al Ma e ials Sec ion Colegio Máximo de Ca uja s/n 18071 – G anada - Spain. Tel.: +34-958243788 Fax: +34-958240809 Email: [email p o ec ed] 37 Figu e 1SI. Figu e 1SI. Con ocal mic og aphs (25 x) ha ep esen ed a 2D maximum p ojec ion o he se ies along ixed axis o he bio ilm a esin-den in in e aces c ea ed using phospho ic acid and a den al adhesi e wi h di e en expe imen al nanopa icles (NPs). a. Specimen wi hou NPs applica ion (con ol) a e 72 h o bac e ial g ow h; b. Undoped nanopa icles (Undoped-NPs) a e 72 h o bio ilm g ow h; c. Bac e ial bio ilm was de eloped du ing 72 h in specimens in which Zn-nanopa icles (Zn-NPs) we e applied; d. Dox-doped nanopa icles (Dox-NPs) we e used; he image was aken a e 72 h o bac e ial g ow h. LIVE/DEAD® BackLigh Bac e ial Viabili y Ki was employed o assess cells in eg i y. Li e cells a e in g een and dead/inju ed cells in ed. Scale ba s a e 30 µm. 38 Figu e 2SI. 39 Figu e 2SI. 2D maps (20 x 20 µm) pe o med a scanning mode by nano-DMA analysis o he complex modulus (E*), a he esin-den in in e ace ea ed wi h Zn-NPs, ob ained a 7 d (a) and 72 h (e, ) ime poin s. In he colo scheme shown, he ed colo co esponds o he highes alue o he locally measu ed moduli, likely co esponding o he highes esis ance o de o ma ion o he in e ubula den in (as e isks). E* e e ed o pe i ubula den in appea s in blue colo (poin e s). The pixel da a a ay a he mapping is o ganized acco ding o E* dis ibu ion ha concu s wi h a clea delimi a ion be ween in e ubula and pe i ubula den in ( aced a ows). Scanning mode nano-DMA analysis o he map o he s o age modulus (E') a he esin-den in in e ace ea ed wi h Zn-NPs a 7 d (b) and Dox-NPs a 72 h ime poin s ( ). In he colo scheme shown, he ed colo co esponds o he highes alue o he locally E' alue moduli, po en ially associa ed o he highes abili y o he in e ubula den in o s o age ene gy, yellowish- ed and yellowish-g een in b and espec i ely, a he mappings. 2D scanning mode nano-DMA analysis o he map o he loss modulus (E") a he esin-den in in e ace ea ed wi h Zn-NPs (c). High loss moduli, o iscous beha io alues (as e isks), we e obse ed in c a in e ubula den in (yellow and ed), in con as wi h he hyb id laye (blue) (poin e s) and he bo om o he hyb id laye (g een) (a ows). 40 Figu e 3SI.