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Duovisc

Manufactured by Alcon
Sourced in United States, Belgium

DuoVisc is a dual-viscosity ophthalmic viscoelastic device designed for use in cataract and intraocular lens (IOL) implantation procedures. It is composed of two distinct viscoelastic formulations, one with a high molecular weight and the other with a low molecular weight, which work together to provide both cohesive and dispersive properties.

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10 protocols using duovisc

1

Standardized Cataract Surgery Procedure

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All surgeries were performed by one experienced surgeon (SWC). Briefly, topical anesthesia was applied with 0.05% proparacaine hydrochloride (ALCAINE, Alcon Laboratories Inc.). With the surgeon sitting superior to the patient, incisions were made at the 12 o'clock position with paracentesis at the 2 o'clock position. A three-step incision was made 0.5 mm posterior to the limbus using a 2.2-mm or 2.75-mm clear corneal knife. A continuous curvilinear capsulorhexis measuring approximately 5.0–5.5 mm in diameter was created after the anterior chamber was inflated with viscoelastic (DuoVisc, Alcon Laboratories Inc.). Nuclei were chopped after hydrodissection, and nuclear fragments were removed by phacoemulsification. In-the-bag implantation of the IOL was completed, and the viscoelastic was then completely removed. Incisions were sealed by standardized stromal hydration at the end of surgery. Only cases with no intraoperative complications were included.
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2

Rat Model of Retinal Detachment and Antioxidant Treatment

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Rats from each group were anesthetized by a mixture of ketamine (75 mg/kg) and xylazine (10 mg/kg) i.p. After cutting the whiskers and eyelashes, disinfecting with iodine solution, and topically anesthetizing with 0.5% proparacaine hydrochloride eye drops to the eye, the pupil was dilated with 5% phenylephrine and 0.5% tropicamide eye drops. The temporal conjunctiva was incised at 5 mm posterior to the limbus and separated from the sclera. For the non-RD group, the tip of a 30 G needle was lightly pierced into the posterior part of the sclera through the incision of the conjunctiva without injection. For the RD group and GTE group, about 2 µL of 1% sodium hyaluronate, DuoVisc® (Alcon-Couvreur, Puurs, Belgium) was injected into the subretinal region through the posterior sclera to induce RD followed by corneal paracentesis with a 30 G needle to normalize the intraocular pressure [8 ]. Fundus photos were taken by the Eyemera Complete Eye Imaging System by IISCIENCE (San Jose, CA, USA) to demonstrate successful RD induction (Figure 2). Both eyes were induced for each rat. Four hours after the induction, the rats from the non-RD group and RD group were intragastrically (i.g.) fed with 0.5 mL water while GTE or EGCG was fed i.g. in an appropriate dose to the treatment groups. They were fed twice daily for three days.
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3

Comparative Pupil Dilation Techniques

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All investigators involved in this study had been selected on the basis of their experience (high volume cataract surgeries for several years) and their acceptance of being videorecorded for the purpose of masked analysis of the pupil size and other endpoints. Additionally, the randomization (ICMA vs. topical eye drops) was performed just before the surgery in order to keep the groups comparable (no possibility of changing the surgeon at the last moment), which was verified (comparable numbers of patients randomized in each group for a given investigator). Mydrane (Laboratoires Théa, Clermont-Ferrand, France) is a commercially available, injectable solution of 1% lidocaine combined with 0.31% phenylephrine and 0.02% tropicamide. Patients in the ICMA Group were injected with 200 μL of ICMA in the anterior chamber just after the first corneal incision. In the Topical Group, the patients received 1 drop each of tropicamide 0.5% and phenylephrine 10%, repeated 3 times at 10-min intervals beginning 30 min before surgery. Preoperatively, both groups received the same regimen of tetracaine 1% (1–2 drops at 5 and 1 min before surgery). Duovisc (Alcon Inc., Fort Worth, TX, USA) viscoelastic was used for all surgeries.
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4

Routine Cataract Surgery Protocol

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A manual 2.75 mm clear corneal incision was created at the 180 degrees meridian in the temporal area. A Surgical Induced Astigmatism of 0.1 was used. The viscoelastic of choice was Duovisc (Alcon). A 5.0–5.5 mm continuous curvilinear capsulorhexis was performed and phacoemulsification was completed in a horizontal chop or divide-and-conquer fashion using the Infiniti Vision System (Alcon Laboratories, Inc., Fort Worth, TX). Manual clear corneal incisions were performed. No capsulotomy complications occurred, and all wounds were confirmed to be self-sealing.
Patients took a topical steroid four times daily and tapered weekly over one month following surgery. A topical NSAID eye drop was used twice daily for six weeks. Third- or fourth-generation fluoroquinolone antibiotic eye drops were used four times daily for one week.
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5

Comparative Evaluation of Ophthalmic Viscosurgical Devices

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We assessed 10 different commercially available OVDs:

Two cohesive OVDs: ProVisc (Alcon, Fort Worth, TX), Z-Hyalin plus (Carl Zeiss Meditec AG, Jena, Germany)

Five dispersive OVDs: Amvisc plus (Bausch & Lomb, Laval, Canada), DisCoVisc (Alcon), Healon EndoCoat (Johnson & Johnson, New Brunswick, NJ), Viscoat (Alcon), Z-Hyalcoat (Carl Zeiss Meditec AG)

And three combination systems: Combivisc (Carl Zeiss Meditec AG), Duo-Visc (Alcon) and Twinvisc (Carl Zeiss Meditec AG).

The specific characteristics of these OVD are shown in Table 1.
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6

Standardized Cataract Surgery Techniques

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The same surgeon (CFVB) performed all surgical procedures employing the standard stop & chop phacoemulsification technique under topical anesthesia. 2.2 mm clear corneal incisions and 5.0 to 5.5 mm manually created capsulorhexes were employed for all surgeries, using the same ophthalmic viscosurgical device (OVD) Duovisc® (3.0% sodium hyaluronate, 4.0% chondroitin sulfate with 1.0% sodium hyaluronate ALCON Laboratories, Forth Worth TX, USA). After cataract removal and cortical material aspiration, all patients had in-the-bag implantation of either an AT LISA tri 839MP or an Acrysof IQ PanOptix in concordance to randomization. Finally, all remaining OVD under the IOL were removed.
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7

Cataract Surgery with Corneal Incision

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A 2.4-mm clear corneal incision was created manually to avoid RK wounds. For patients with an increased risk of their RK incision opening with a corneal incision, a scleral approach was employed. Astigmatism of 0.1 was surgically induced. Duovisc (Alcon Laboratories, Inc., Fort Worth, TX, USA) viscoelastic was used. The surgeon performed a continuous curvilinear capsulorhexis ranging from 5.0 to 5.55 mm in size. Phacoemulsification, either in a horizontal chop or divide-and-conquer fashion, was carried out using the Infiniti Vision System (Alcon Laboratories, Inc). There were no complications related to the capsulotomy. Lenses were chosen by selecting the power that most closely approximated emmetropia, which was also the lowest myopic correction. All wounds were confirmed to be self-sealing.
Post-surgery, patients were instructed to use topical steroids 4 times a day, gradually tapering the dosage on a weekly basis over the course of 1 month. They were also advised to use topical non-steroid anti-inflammatory drug (NSAID) eyedrops twice daily for 6 weeks. Additionally, third- or fourth-generation fluoroquinolone antibiotic eyedrops were prescribed to be used 4 times daily for 1 week.
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8

Green Tea Extract Bioactive Profiling

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The green tea extract (GTE), Theaphenon E®, kindly provided by Dr. Yukihiko Hara, contained 70% epigallocatechin gallate (EGCG), 5% epigallate catechins (EGC), 4% epicatechin (EC), and 0.6% gallocatechin (GC) [5 (link)]. Sodium hyaluronate (1%) (DuoVisc®) was obtained from Alcon-Couvreur (Puurs, Belgium). Total protein assay was obtained from PierceTM BCA Protein Assay Kit (Rockford, IL, USA). The TUNEL assay kit was purchased from ABCAM (Waltham, MA, USA). The Rat Caspase-3 ELISA Kit was obtained from CUSABIO (Houston, TX, USA). The Protein Carbonyl Content Assay Kit was purchased from ABCAM (Waltham, MA, USA). The Rat MCP-1 instant ELISATM Kits were obtained from InvitrogenTM (Vienna, Austria). The Rat XL Cytokine Array Kit of Proteome ProfilerTM Array was purchased from the R&D system (McKinley Place, MN, USA). Fatty acid methyl ester C4–C24 standard mixture and BSTFA+TMCS (99:1) were obtained from Supelco (Bellefonte, PA, USA). Cholesterol, Cholesterol-2,3,4-13C3, and palmitic acid-d31 were purchased from Sigma-Aldrich (St. Louis, MO, USA). Decanoic acid-d19 was obtained from Cambridge Bioscience (Cambridge, UK). Trimethylsilydiazomethane was purchased from Alfa Aesar (Lancashire, UK). All other reagents were of the highest grade available.
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9

Tissue Preparation for Microscopy

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For observations of living tissues, the whole living MucilAir™/OncoCilAir™ tissues was removed from its cell culture insert and placed on a microscopic slide. A Viscoelastic System (Viscot, DuoVisc, Alcon) containing hyaluronate de sodium, chondroitin sulfate was added on the tissue for minimizing the cell stress during coverslip mounting. The tissue was then gently flattened using a large glass coverslip retained by adhesive tape.
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10

Standardized Phacoemulsification Procedure

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All surgeries were performed by one experienced surgeon (J-MP). As described previously [50 (link)], the patients were given topical anesthesia, pupillary dilation was induced, a blepharostat was positioned, a coaxial 2.2-mm corneal mini-incision was created, dispersive viscoelastic (DuoVisc; Alcon Laboratories, Switzerland) was injected into the anterior chamber, a second incision (90° to the first incision) was generated with a 20-gauge needle, circular capsulorhexis was conducted, and lens-nucleus hydrodissection was performed with either DAC [49 (link)] or subluxation [47 (link), 48 (link)]. All phacoemulsifications were performed with the same machine (Stellaris; Bausch & Lomb, Inc., Canada) with the following parameters: 450 mmHg vacuum, 35 cc/min fixed aspiration rate, 110-cm bottle height, and 60–40% phacopower. After phacoemulsification, an acrylic intraocular lens was implanted, viscoelastic was completely removed with irrigation and aspiration, and the corneal incision was gently hydrated. Surgery was completed with a corneal stitch if required and patients were given an intracameral injection of cefuroxime (Aprokam; Laboratoires Théa, France).
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